BAXTER INTERNATIONAL INC
For the period ended Sep 30, 2026. Filed Oct 29, 2026.
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A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.
Sep 30, 2026 · Filed Oct 29, 2026
What changed in Management’s Discussion and Analysis?
Read the current filingPrevious report: 10-Q
Period ended 2026-06-30; filed 2026-07-30.
0001628280-26-051118
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of OperationsCurrent report: 10-Q
Period ended 2026-09-30; filed 2026-10-29.
0001628280-26-068278
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of OperationsThe baseline is this issuer’s latest earlier reporting period of the same form that was filed before the current report. A previous 10-Q is a different quarter, not a year-over-year comparison. Amendments are excluded.
Compared 172 previous paragraphs and 176 current paragraphs.
97 unchanged; 71 reworded; 6 added; 4 removed; 0 previous and 2 current paragraphs rearranged.
Tables are not compared: 11 previous and 11 current tables excluded. Dates, whitespace, punctuation and numbering changes are ignored; changes to financial figures remain significant.
A changed paragraph is not evidence that risk increased or decreased. An unchanged paragraph does not establish that risk stayed the same.
Added paragraphs (6)
Current report
ONGOING BUSINESS TRANSFORMATION
Current report
Net income (loss) attributable to Baxter stockholders for the three months ended September 30, 2026 was $294 million, or $0.57 per diluted share, compared to $(46) million, or $(0.09) per diluted share for the three months ended September 30, 2025. For the three months ended September 30, 2026, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $5 million, or $0.01 per diluted share. For the three months ended September 30, 2025, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $401 million, or $0.78 per diluted share.
Current report
For the nine months ended September 30, 2025, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $780 million, or $1.52 per diluted share.
Current report
9 Our results for the third quarter and the first nine months of 2026 included a gain of $253 million on the early extinguishment of debt. Refer to Note 5 in Item 1 of this Quarterly Report on Form 10-Q for further information on the debt repayments.
Current report
For the three months ended September 30, 2025, the difference between our effective income tax rate and the U.S. federal statutory rate was primarily driven by an increase in liabilities for uncertain tax positions, partially offset by a reduction in the valuation allowance on foreign tax credits and changes in the treatment of accumulated earnings that are considered indefinitely reinvested as of December 31, 2024.
Current report
In March 2026, FDA commenced an inspection of our sterile injectable drug manufacturing facility in Round Lake, Illinois (Round Lake). Upon completion of the inspection in April 2026, FDA issued a Form-483 providing a list of observations. In June 2026, Round Lake received an OAI classification following the inspection. In September 2026, FDA issued a Warning Letter (2026 Warning Letter)3 based on the observations identified in the inspection. In October 2026, we responded to the 2026 Warning Letter and are continuing to implement corrective and preventive actions to address FDA’s observations as set forth in the 2026 Warning Letter and the related Form 483.
Removed paragraphs (4)
Previous report
COMPLETED STRATEGIC ACTION; ONGOING BUSINESS TRANSFORMATION
Previous report
Net income (loss) attributable to Baxter stockholders for the three months ended June 30, 2026 was $126 million, or $0.24 per diluted share, compared to $91 million, or $0.18 per diluted share for the three months ended June 30, 2025. For the three months ended June 30, 2026, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $155 million, or $0.30 per diluted share. For the three months ended June 30, 2025, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $185 million, or $0.36 per diluted share.
Previous report
2025, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $379 million, or $0.74 per diluted share.
Previous report
For the three months ended June 30, 2025, the difference between our effective income tax rate and the U.S. federal statutory rate was primarily driven by our global earnings mix.
Reworded paragraphs (71)
Previous wording
Refer to our Annual Report on Form 10-K for the year ended December 31, 2025 (2025 Annual Report) for management’s discussion and analysis of our financial condition and results of operations. The following is management’s discussion and analysis of our financial condition and results of operations for the three and six months ended June 30, 2026 and 2025.
Current wording
Refer to our Annual Report on Form 10-K for the year ended December 31, 2025 (2025 Annual Report) for management’s discussion and analysis of our financial condition and results of operations. The following is management’s discussion and analysis of our financial condition and results of operations for the three and nine months ended September 30, 2026 and 2025.
Previous wording
We have incurred and expect to incur additional dis-synergies following our sale of our Kidney Care business due to the reduced size of our company and, as a result, we have undertaken certain restructuring actions (and intend to undertake additional actions) to help ensure our cost structuring is appropriate to support our remaining business. See Note 10 of this Quarterly Report on Form 10-Q for additional information.
Current wording
We have incurred and expect to incur additional dis-synergies following our sale of our Kidney Care business due to the reduced size of our company and, as a result, we have undertaken certain restructuring actions (and intend to undertake additional actions) to help ensure our cost structure is appropriate to support our remaining business. See Note 10 of this Quarterly Report on Form 10-Q for additional information.
Previous wording
During 2025, we initiated voluntary corrections for the Novum LVP. The U.S. Food and Drug Administration (FDA) classified these voluntary corrections as Class I recalls. We have implemented certain corrections related to the recalls and have identified additional corrections to address these recalls, some of which may require regulatory clearance or approval, and are in the early stages of verification testing. In July 2025, we elected to temporarily stop distributing and installing the Novum LVP in the U.S. and Canada, except in the case of medical necessity. The timing of the release of the shipment and installation hold remains uncertain. As a result, we expect no meaningful sales of Novum LVP while these holds are in effect. Our Spectrum IQ large volume pump remains available as an alternative option for customers with Novum LVPs. In 2025, we recorded estimates for sales reductions, for returns or exchanges of Novum LVP, and certain other charges, including estimates of reserves for remediation costs and inventory and contract asset write-downs associated with these Novum LVP corrections. We regularly review these estimates (including those associated with any future additional corrections and customer returns or exchanges), which may be subject to additional change in the future. In the first quarter of 2026, we adjusted certain estimates associated with these Novum LVP corrections that were not material to our condensed consolidated financial statements; no such adjustments were recorded in the second quarter of 2026.
Current wording
During 2025, we initiated voluntary corrections for the Novum LVP. The U.S. Food and Drug Administration (FDA) classified these voluntary corrections as Class I recalls. We have implemented certain corrections related to the recalls and have identified additional corrections to address these recalls, some of which may require regulatory clearance or approval, and are in the early stages of verification testing. In July 2025, we elected to temporarily stop distributing and installing the Novum LVP in the U.S. and Canada, except in the case of medical necessity. The timing of the release of the shipment and installation hold remains uncertain. As a result, we expect no meaningful sales of Novum LVP while these holds are in effect. Our Spectrum IQ large volume pump remains available as an alternative option for customers with Novum LVPs. In 2025, we recorded estimates for sales reductions, for returns or exchanges of Novum LVP, and certain other charges, including estimates of reserves for remediation costs and inventory and contract asset write-downs associated with these Novum LVP corrections. We regularly review these estimates (including those associated with any future additional corrections and customer returns or exchanges), which may be subject to additional change in the future. In the first quarter of 2026, we adjusted certain estimates associated with these Novum LVP corrections that were not material to our condensed consolidated financial statements; no such adjustments were recorded in the second and third quarters of 2026.
Previous wording
We have experienced challenges to our global supply chain, including, as a result of adverse impacts from significant weather events like Hurricane Helene and other global macroeconomic and geopolitical events (including the ongoing conflict in Iran), which have had a negative impact on our results of operations and may do so in the future. In addition, announcements regarding changes in U.S. trade policies and practices, including the implementation of global tariffs and proposed further tariffs (including potential medical device and pharmaceutical tariffs), the Supreme Court's decision to invalidate tariffs levied under the International Emergency Economic Powers Act (IEEPA), and responses from other jurisdictions, have significantly affected financial markets and economic conditions. In the second quarter of 2026, we recorded tariff refunds of approximately $75 million to costs of goods sold in our condensed consolidated statements of income (loss) (which is inclusive of $65 million in prepaid expenses and other current assets) for probable receipt of amounts eligible for refund in the first and second phases of the process and expect to submit additional refund requests in future phases subject to further rulings by the Court of International Trade. While uncertainty remains surrounding the timing of any additional amounts we may ultimately recover on current or future refund claims, we do not expect for any additional amounts to be material to our condensed consolidated financial statements. We currently expect that our results will continue to be adversely impacted by Section 122 duties and recently announced Section 301 tariffs that have been imposed following the judicial review of certain tariffs. Additionally, continued global macroeconomic uncertainty, including in trade policies and practices, elevated tariffs and operational and policy changes in the governments of the U.S. and other countries and other geopolitical events or conflicts (including the ongoing conflict in Iran and the potential for escalation of this and other conflicts), could contribute to further market volatility, deteriorating or prolonged weakened economic conditions and decreased hospital capital spending levels. We continue to closely monitor these developing situations and the estimated impact on our business, results of operations, financial condition and cash flows.
Current wording
We have experienced challenges to our global supply chain, including, as a result of adverse impacts from significant weather events like Hurricane Helene and other global macroeconomic and geopolitical events (including the ongoing conflict in Iran and the potential for escalation of this and other conflicts), which have had a negative impact on our results of operations and may do so in the future. In addition, announcements regarding changes in U.S. trade policies and practices, including the implementation of global tariffs and proposed further tariffs (including potential medical device and pharmaceutical tariffs), the Supreme Court's decision to invalidate tariffs levied under the International Emergency Economic Powers Act (IEEPA), and responses from other jurisdictions, have significantly affected financial markets and economic conditions. In the second quarter of 2026, we recorded tariff refunds of approximately $75 million to costs of goods sold in our condensed consolidated statements of income (loss) (which was substantially collected during the third quarter of 2026) for probable receipt of amounts eligible for refund in the first and second phases of the process and expect to submit additional refund requests in future phases subject to further rulings by the Court of International Trade. While uncertainty remains surrounding the timing of any additional amounts we may ultimately recover on current or future refund claims, we do not expect for any additional amounts to be material to our condensed consolidated financial statements. We currently expect that our results will continue to be adversely impacted by Section 122 duties and previously announced Section 301 tariffs. Additionally, continued global macroeconomic uncertainty, including in trade policies and practices, elevated tariffs and operational and policy changes in the governments of the U.S. and other countries and other geopolitical events or conflicts, could contribute to further market volatility, deteriorating or prolonged weakened economic conditions and decreased hospital capital spending levels. We continue to closely monitor these developing situations and the estimated impact on our business, results of operations, financial condition and cash flows.
Previous wording
Over the past few years, the existence of high inflation rates in the United States and in many of the countries where we conduct business has resulted in, and may in the future result in, higher interest rates, shipping costs, labor costs, and other costs and expenses. Additionally, adverse changes in foreign currency exchange rates have increased, and could continue to increase, our costs of sourcing certain raw materials in some jurisdictions. We have experienced and are likely in the future to continue to experience inflationary and other increases in manufacturing costs and operating expenses (including as a result of the aforementioned tariffs and conflicts) and are limited in our ability to pass these cost increases on to our customers in a timely manner or at all due to the longer term nature of our customer contracts and arrangements, which could have a material adverse impact on our profitability and results of operations. Inflation and general macroeconomic factors have caused certain of our customers to reduce or delay orders for our products and services and could cause them to do so in the future, which could have a material adverse impact on our sales and results of operations.
Current wording
Over the past few years, the existence of high inflation rates in the United States and in many of the countries where we conduct business has resulted in, and are likely in the future to result in, higher interest rates, shipping costs, labor costs, and other costs and expenses. Additionally, adverse changes in foreign currency exchange rates have increased, and could continue to increase, our costs of sourcing certain raw materials in some jurisdictions. We have experienced and are likely in the future to continue to experience inflationary and other increases in manufacturing costs and operating expenses (including as a result of the aforementioned tariffs and conflicts) and are limited in our ability to pass these cost increases on to our customers in a timely manner or at all due to the longer term nature of our customer contracts and arrangements. We are also limited in our ability to switch suppliers given the regulated nature of our products and the lead times associated with qualifying new suppliers. These constraints could have a material adverse impact on our profitability and results of operations. Inflation and general macroeconomic factors have caused certain of our customers to reduce or delay orders for our products and services and could cause them to do so in the future, which could also have a material adverse impact on our sales and results of operations.
Previous wording
Net income (loss) attributable to Baxter stockholders for the six months ended June 30, 2026 was $111 million, or $0.21 per diluted share, compared to $217 million, or $0.42 per diluted share for the six months ended June 30, 2025. For the six months ended June 30, 2026, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $360 million, or $0.70 per diluted share. For the six months ended June 30,
Current wording
Net income (loss) attributable to Baxter stockholders for the nine months ended September 30, 2026 was $405 million, or $0.78 per diluted share, compared to $171 million, or $0.33 per diluted share for the nine months ended September 30, 2025. For the nine months ended September 30, 2026, our results included special items that adversely impacted net income (loss) attributable to Baxter stockholders by $365 million, or $0.71 per diluted share.
Previous wording
Net income (loss) from continuing operations for the three months ended June 30, 2026 was $135 million, or $0.26 per diluted share, compared to $122 million, or $0.24 per diluted share for the three months ended June 30, 2025. Net income (loss) from continuing operations for the three months ended June 30, 2026 included special items that adversely impacted net income (loss) by $155 million, or $0.30 per diluted share. Net income (loss) from continuing operations for the three months ended June 30, 2025 included special items that adversely impacted net income (loss) by $182 million, or $0.35 per diluted share.
Current wording
Net income (loss) from continuing operations for the three months ended September 30, 2026 was $298 million, or $0.57 per diluted share, compared to $(51) million, or $(0.10) per diluted share for the three months ended September 30, 2025. Net income (loss) from continuing operations for the three months ended September 30, 2026 included special items that adversely impacted net income (loss) by $5 million, or $0.01 per diluted share. Net income (loss) from continuing operations for the three months ended September 30, 2025 included special items that adversely impacted net income (loss) by $404 million, or $0.79 per diluted share.
Previous wording
Net income (loss) from continuing operations for the six months ended June 30, 2026 was $118 million, or $0.23 per diluted share, compared to $186 million, or $0.36 per diluted share for the six months ended June 30, 2025. Net income (loss) from continuing operations for the six months ended June 30, 2026 included special items that adversely impacted net income (loss) by $360 million, or $0.69 per diluted share. Net income (loss) from continuing operations for the six months ended June 30, 2025 included special items that adversely impacted net income (loss) by $403 million, or $0.79 per diluted share.
Current wording
Net income (loss) from continuing operations for the nine months ended September 30, 2026 was $416 million, or $0.80 per diluted share, compared to $135 million, or $0.26 per diluted share for the nine months ended September 30, 2025. Net income (loss) from continuing operations for the nine months ended September 30, 2026 included special items that adversely impacted net income (loss) by $365 million, or $0.71 per diluted share. Net income (loss) from continuing operations for the nine months ended September 30, 2025 included special items that adversely impacted net income (loss) by $807 million, or $1.57 per diluted share.
Previous wording
In the second quarter of 2026, the Kidney Care MSA sales adversely impacted sales growth by 1% and foreign exchange rates favorably impacted net sales growth by 1%, compared to the prior year period due to the strengthening of the U.S. Dollar relative to the Australian Dollar, Euro, Colombian Peso and Brazilian Real. In the first six months of 2026, the foreign currency rates favorably impacted net sales growth by 2%, compared to the prior year period due to the strengthening of the U.S. Dollar relative to the Euro, Australian Dollar, British Pound, Brazilian Real, Colombian Peso, and Canadian Dollar.
Current wording
In the third quarter of 2026, the Kidney Care MSA sales adversely impacted sales growth by 1% and foreign exchange rates favorably impacted net sales growth by 1%, compared to the prior year period due to the weakening of the U.S. Dollar relative to the Australian Dollar and Colombian Peso, partially offset by the strengthening of the U.S. Dollar relative to the Euro. In the first nine months of 2026, the Kidney Care MSA sales adversely impacted sales growth by 1% and foreign currency rates favorably impacted net sales growth by 2%, compared to the prior year period due to the weakening of the U.S. Dollar relative to the Australian Dollar, Euro, Colombian Peso, British Pound, Brazilian Real, and Mexican Peso, partially offset by the strengthening of the U.S. Dollar relative to the Turkish Lira.
Previous wording
Medical Products & Therapies segment net sales increased 7% in the second quarter and increased 5% in the first six months of 2026, as compared to the prior year periods.
Current wording
Medical Products & Therapies segment net sales increased 6% in the third quarter and first nine months of 2026, as compared to the prior year periods.
Previous wording
Infusion Therapies & Platforms net sales increased 6% in the second quarter and increased 4% in the first six months of 2026, as compared to the prior year periods. The increase in the second quarter was driven by increased demand for our international pharmacy compounding offerings and a weak prior year comparison in the U.S. IV solutions business, during which we experienced lower sales due to distributor destocking and fluid conservation practices embedded with clinical practice changes. These increases were partially offset by a sales decline in our Injectables portfolio due to ongoing supply constraints in the U.S. and international markets and softness in certain premix products. Sales volumes were further impacted by lower volumes of our Novum LVP due to the continued shipment and implementation hold. Foreign exchange rates favorably impacted sales growth by 2% for the second quarter of 2026, as compared to the prior year period. Sales performance in the first six months of 2026 reflected increased demand for our international pharmacy compounding offerings, partially offset by lower sales in our injectables portfolio due to ongoing supply constraints in the U.S. and international markets and softness in certain premix products, as well as lower volumes of our Novum LVP due to the continued shipment and implementation hold. Foreign exchange rates favorably impacted sales growth by 3% for the first six months of 2026, as compared to the prior year period. As previously discussed in "Factors Affecting our Results of Operations", we elected to temporarily stop distributing and installing the Novum LVP in the U.S. and Canada, except in the case of medical necessity. As a result, we expect no meaningful sales of Novum LVP while these holds are in effect. Our Spectrum IQ large volume pump remains available as an alternative option for customers with Novum LVPs.
Current wording
Infusion Therapies & Platforms net sales increased 5% in the third quarter and increased 4% in the first nine months of 2026, as compared to the prior year periods. The increase in the third quarter was driven by sales of our Spectrum IQ pump, contributions from our portfolio of digital solutions and administrative sets portfolio. Sales volumes were further driven by increased demand for our international pharmacy compounding offerings and growth in the U.S. IV solutions business reflecting a lower baseline level of demand following clinical practice changes in the market, partially offset by lower sales in our Injectables portfolio. Foreign exchange rates favorably impacted sales growth by 1% for the third quarter of 2026, as compared to the prior year period. Sales performance in the first nine months of 2026 reflected increased demand for our international pharmacy compounding offerings, partially offset by lower sales in our Injectables portfolio due to ongoing supply constraints in the U.S. and international markets. Foreign exchange rates favorably impacted sales growth by 2% for the first nine months of 2026, as compared to the prior year period. As previously discussed in "Factors Affecting our Results of Operations", we elected to temporarily stop distributing and installing the Novum LVP in the U.S. and Canada, except in the case of medical necessity. As a result, we expect no meaningful sales of Novum LVP while these holds are in effect. Our Spectrum IQ large volume pump remains available as an alternative option for customers with Novum LVPs.
Previous wording
Advanced Surgery net sales increased 12% in the second quarter and increased 13% in the first six months of 2026, as compared to the prior year periods. Sales performance was primarily driven by growth in hemostats and sealants and was primarily attributable to increased sales volume globally. Foreign currency exchange rates favorably impacted sales growth by 2% in the first six months of 2026, as compared to the prior year period.
Current wording
Advanced Surgery net sales increased 12% in the third quarter and first nine months of 2026, as compared to the prior year periods. Sales performance was primarily driven by growth in hemostats and sealants and was primarily attributable to increased sales volume globally. Foreign currency exchange rates favorably impacted sales growth by 1% in the first nine months of 2026, as compared to the prior year period.
Previous wording
Our Healthcare Systems & Technologies segment includes sales of our connected care solutions and collaboration tools, including smart bed systems, patient monitoring systems and diagnostic technologies, respiratory health devices, and advanced equipment for the surgical space, including operating room integration technologies, precision positioning devices, and other accessories.
Current wording
Our Healthcare Systems & Technologies segment includes sales of our connected care solutions and collaboration tools, including smart bed systems, connected monitoring systems, formerly known as patient monitoring systems, and diagnostic technologies, respiratory health devices, and advanced equipment for the surgical space, including operating room integration technologies, precision positioning devices, and other accessories.
Previous wording
Healthcare Systems & Technologies segment net sales increased 4% in the second quarter and increased 2% in the first six months of 2026, as compared to the prior year periods.
Current wording
Healthcare Systems & Technologies segment net sales increased 4% in the third quarter and increased 3% in the first nine months of 2026, as compared to the prior year periods.
Previous wording
Care & Connectivity Solutions net sales increased 6% in the second quarter and increased 4% in the first six months of 2026, as compared to the prior year periods. Sales performance was primarily driven by increased volume associated with execution against the order backlog in the U.S. for patient support systems. Foreign currency exchange rates favorably impacted sales growth by 1% for the second quarter and the first six months of 2026, as compared to the prior year periods.
Current wording
Care & Connectivity Solutions net sales increased 5% in the third quarter and increased 4% in the first nine months of 2026, as compared to the prior year periods. The increase in the third quarter was primarily driven by acceleration of our global surgical solutions business and increased volume associated with partial execution against the order backlog in the U.S. for patient support systems. The increase in the first nine months was primarily driven by increased volume associated with execution against the order backlog in the U.S. for patient support systems and acceleration of our global surgical solutions business.
Previous wording
Front Line Care net sales increased 2% in the second quarter and were flat in the first six months of 2026, as compared to the prior year periods. The increase in the second quarter was primarily impacted by continued momentum within patient monitoring systems and the timing of orders, partially offset by planned global product exits. Sales performance in the first six months was driven by increased demand across our respiratory health products, confirm cardiology products and patient monitoring systems, offset by planned global product exits. Foreign currency exchange rates favorably impacted sales growth by 1% the first six months of 2026, as compared to the prior year period.
Current wording
Front Line Care net sales increased 3% in the third quarter and increased 1% in the first nine months of 2026, as compared to the prior year periods. The increase in the third quarter was primarily impacted by continued momentum within connected monitoring systems, partially offset by planned global product exits. The increase in the first nine months was driven by increased demand across our connected monitoring systems and respiratory health products, partially offset by planned global product exits. Foreign currency exchange rates favorably impacted sales growth by 1% the first nine months of 2026, as compared to the prior year period.
Previous wording
Other sales, which represent sales not allocated to a reportable segment, include sales to Vantive, pursuant to the Kidney Care MSA. During the three months ended June 30, 2026 and 2025, we earned $83 million and $98 million, and $159 million and $161 million for the six months ended June 30, 2026 and 2025, respectively, of revenues that were not attributable to our reportable segments. The decrease in Other sales for the second quarter and six months ended June 30, 2026 as compared to the prior year periods is driven by reduced volumes under the Kidney Care MSA.
Current wording
Other sales, which represent sales not allocated to a reportable segment, include sales to Vantive, pursuant to the Kidney Care MSA. During the three months ended September 30, 2026 and 2025, we earned $68 million and $85 million, and $227 million and $246 million for the nine months ended September 30, 2026 and 2025, respectively, of revenues that were not attributable to our reportable segments. The decrease in Other sales for the third quarter and nine months ended September 30, 2026 as compared to the prior year periods is driven by reduced volumes under the Kidney Care MSA.
Previous wording
The following table provides a summary of our special items from continuing operations and the related impact by line item on our results for the three and six months ended June 30, 2026 and 2025.
Current wording
The following table provides a summary of our special items from continuing operations and the related impact by line item on our results for the three and nine months ended September 30, 2026 and 2025.
Previous wording
1 Our results for the second quarter of 2026 and 2025 included business optimization charges of $7 million and $17 million, respectively. Our results for the first six months of 2026 and 2025 included business optimization charges of $75 million and $62 million, respectively. These restructuring and business optimization costs primarily related to initiatives to reduce our cost structure following the sale of our former Kidney Care business. Refer to Note 10 in Item 1 of this Quarterly Report on Form 10-Q for further information regarding these charges and related liabilities.
Current wording
1 Our results for the third quarter of 2026 and 2025 included $61 million and $38 million, respectively, and for the first nine months of 2026 and 2025 included $136 million and $100 million, respectively, of business optimization charges. These restructuring and business optimization charges in the third quarter and first nine months of 2026 included costs primarily related to our initiatives to reduce our cost structure following the sale of our former Kidney Care business and the cessation of production of certain products at one of our specialty injectables manufacturing facilities. These restructuring and business optimization charges in the third quarter and first nine months of 2025 included costs primarily related to our initiatives to reduce our cost structure following the sale of our former Kidney Care business and the exit of a product line at one of our manufacturing facilities. Refer to Note 10 in Item 1 of this Quarterly Report on Form 10-Q for further information regarding these charges and related liabilities.
Previous wording
2 Our results for the second quarter of 2026 and 2025 included $4 million and $5 million, respectively, and for the first six months of 2026 and 2025 included $8 million and $10 million, respectively, of incremental costs to comply with the European Union's medical device regulations for previously registered products, which primarily consist of contractor costs and other direct third-party costs. We consider the adoption of these regulations to be a significant one-time regulatory change and believe that the costs of initial compliance for previously registered products over the implementation period are not indicative of our core operating results.
Current wording
2 Our results for the third quarter of 2026 and 2025 included $3 million and $5 million, respectively, and for the first nine months of 2026 and 2025 included $11 million and $15 million, respectively, of incremental costs to comply with the European Union's medical device regulations for previously registered products, which primarily consist of contractor costs and other direct third-party costs. We consider the adoption of these regulations to be a significant one-time regulatory change and believe that the costs of initial compliance for previously registered products over the implementation period are not indicative of our core operating results.
Previous wording
3 Our results for the first six months of 2026 included a benefit of $12 million related to a revised estimate of warranty and remediation activities from field corrective actions across our infusion pump category initially recorded in 2025. Our results for the second quarter and first six months of 2025 included charges of $23 million and $29 million, respectively, related to an estimate of warranty and remediation activities from field corrective actions on certain of our infusion pumps and a revised estimate of warranty and remediation activities arising from a field corrective action on certain of our infusion pumps initially recorded in 2022.
Current wording
3 Our results for the first nine months of 2026 included a benefit of $12 million related to a revised estimate of warranty and remediation activities from field corrective actions across our infusion pump category initially recorded in 2025. Our results for the third quarter and first nine months of 2025 included charges of $32 million and $61 million, respectively, related to estimates of warranty and remediation activities from field corrective actions on certain of our infusion pumps and a revised estimate of warranty and remediation activities arising from a field corrective action on certain of our infusion pumps initially recorded in 2022.
Previous wording
4 Our results in the second quarter and the first six months of 2026 included charges of $23 million and $34 million, respectively, primarily related to business transformation costs which include expenses incurred in connection with discrete, recently launched enterprise‑wide initiatives to modernize and simplify systems, redesign operating models, and enhance process efficiency and digital capabilities. These costs are distinct from restructuring‑related charges (which are included in footnote 1 above as Business Optimization items) and are excluded to provide investors with greater comparability of underlying operating performance.
Current wording
4 Our results in the third quarter and the first nine months of 2026 included charges of $20 million and $54 million, respectively, primarily related to business transformation costs which include external expenses incurred in connection with discrete, recently launched enterprise‑wide initiatives to modernize and simplify systems, redesign operating models, and enhance process efficiency and digital capabilities. These costs are distinct from restructuring‑related charges (which are included in footnote 1 above as Business Optimization items) and are excluded to provide investors with greater comparability of underlying operating performance.
Previous wording
5 Our results in the second quarter of 2026 and 2025 included charges of $3 million and $17 million, respectively, and for the first six months of 2026 and 2025 included $6 million and $115 million, respectively, related to damages caused by Hurricane Helene which consisted of remediation, air freight and other costs.
Current wording
5 Our results in the third quarter of 2026 and 2025 included charges of $3 million and $8 million, respectively, and for the first nine months of 2026 and 2025 included $9 million and $123 million, respectively, related to damages caused by Hurricane Helene which consisted of remediation, air freight and other costs.
Previous wording
6 Our results in the first six months of 2025 included charges of $11 million related to matters involving alleged injury from environmental exposure.
Current wording
6 Our results in the third quarter and first nine months of 2026 included a net benefit of $27 million. This includes a gain recognized primarily from the settlement of certain patent infringement claims, partially offset with a loss recognized from the settlement of certain patent infringement claims and related fees associated with these matters. Our results for the first nine months of 2025 included charges of $11 million related to matters involving alleged injury from environmental exposure.
Previous wording
7 Our results for the second quarter and first six months of 2025 included $5 million and $11 million, respectively, of integration costs which primarily reflected third party consulting costs related to the ongoing integration of Hill-Rom Holdings, Inc. (Hillrom). In the first six months of 2025 those costs also included the recognition of a non-cash impairment of property, plant and equipment related to integration activities.
Current wording
7 Our results for the third quarter and first nine months of 2025 included $8 million and $19 million, respectively, of integration costs which primarily reflected third party consulting costs related to the ongoing integration of Hill-Rom Holdings, Inc. (Hillrom). In the first nine months of 2025 those costs also included the recognition of a non-cash impairment of property, plant and equipment related to integration activities.
Previous wording
8 Our results for the second quarter of 2026 and 2025 included $22 million and $14 million, respectively, and for the first six months of 2026 and 2025 included $33 million and $27 million, respectively of separation-related costs primarily reflecting costs of external advisors supporting our activities related to the sale of our former Kidney Care business.
Current wording
8 Our results for the third quarter of 2026 and 2025 included $2 million and $13 million, respectively, and for the first nine months of 2026 and 2025 included $35 million and $40 million, respectively of separation-related costs primarily reflecting costs of external advisors supporting our activities related to the sale of our former Kidney Care business.
Previous wording
9 Our results in the first six months of 2026 and 2025 included $5 million and $9 million, respectively, related to losses from non-cash impairment write-downs of investments.
Current wording
10 Our results in the first nine months of 2026 and 2025 included $5 million and $9 million, respectively, related to losses from non-cash impairment write-downs of investments.
Previous wording
10 Our results in the second quarter of 2026 included a $3 million income tax benefit related to the settlement of certain income tax audits and adjustments to our valuation allowance on U.S. deferred tax assets, partially offset by the application of intraperiod tax allocation to our adjusted results in an interim period. Our results in the second quarter of 2025 included $4 million of income tax expense resulting from the application of an intraperiod tax allocation to our adjusted results in an interim period. Our results in the first six months of 2026 included $23 million of income tax expense primarily related to differences arising from the use of a forecasted effective tax rate to compute income tax expense during the period, partially offset by the settlement of certain income tax audits. Our results in the first six months of 2025 included $39 million of income tax benefit primarily driven by an entity classification election that we made for U.S. tax purposes, which resulted in a capital loss.
Current wording
11 Our results in the third quarter of 2026 included $41 million income tax expense primarily related to the application of intraperiod tax allocation to our adjusted results in an interim period. Our results in the first nine months of 2026 included $64 million of income tax expense primarily related to differences arising from the use of a forecasted effective tax rate to compute income tax expense during the period, partially offset by the settlement of certain income tax audits and adjustments to the U.S. valuation allowance. Our results in the third quarter of 2025 included $213 million of income tax expense primarily related to an increase in reserves for uncertain tax positions and a step-up in Swiss valuation allowances, partially offset by the release of valuation allowances on foreign tax credits. Our results in the first nine months of 2025 included $174 million of income tax expense primarily related to an increase in reserves for uncertain tax positions and a step-up in Swiss valuation allowances, partially offset by the release of valuation allowances on foreign tax credits and an entity classification election that we made for U.S. tax purposes, which resulted in a capital loss.
Previous wording
11 This item reflects the income tax impact of the special items identified in this table. The tax effect of each special item is based on the jurisdiction in which the item was incurred and the tax laws in effect for each such jurisdiction.
Current wording
12 This item reflects the income tax impact of the special items identified in this table. The tax effect of each special item is based on the jurisdiction in which the item was incurred and the tax laws in effect for each such jurisdiction.
Previous wording
Our gross margin ratio was 34.9% and 35.3% for the three months ended June 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 3.7 and 5.4 percentage points on the gross margin ratio for the three months ended June 30, 2026 and 2025, respectively. Our gross margin ratio was 34.0% and 34.1% for the first six months ended June 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 3.7 and 7.2 percentage points on the gross margin ratio for the first six months ended June 30, 2026 and 2025, respectively.
Current wording
Our gross margin ratio was 33.4% and 33.5% for the three months ended September 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 4.9 and 5.9 percentage points on the gross margin ratio for the three months ended September 30, 2026 and 2025, respectively. Our gross margin ratio was 33.8% and 33.9% for the first nine months ended September 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 4.1 and 6.7 percentage points on the gross margin ratio for the first nine months ended September 30, 2026 and 2025, respectively.
Previous wording
Excluding the impact of special items, the gross margin ratio decreased by 2.1 and 3.6 percentage points in the second quarter and first six months of 2026, respectively, compared to the prior year periods. The lower gross margins were primarily driven by increased manufacturing and supply costs, including an updated estimate of indirect costs previously recorded in SG&A now capitalized into inventory after the separation of our former Kidney Care business, and product mix, partially offset by IEEPA tariff refunds recorded in the second quarter of 2026.
Current wording
Excluding the impact of special items, the gross margin ratio decreased by 1.1 percentage points in the third quarter of 2026 compared to the prior year period, primarily due to unfavorable product mix and a lower contribution from pricing. Excluding the impact of special items, the gross margin ratio decreased by 2.7 percentage points in the first nine months of 2026 compared to the prior year period, primarily due to increased manufacturing and supply costs, unfavorable product mix and lower contribution from pricing, partially offset by IEEPA tariff refunds recorded in the second quarter of 2026.
Previous wording
Our SG&A expenses ratio was 24.8% and 25.6% for the three months ended June 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 2.9 percentage points on the SG&A expenses ratio for the three months ended June 30, 2026 and 2025. Our SG&A expenses ratio was 25.8% and 26.1% for the first six months ended June 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 3.5 and 3.2 percentage points on the SG&A expenses ratio for the first six months ended June 30, 2026 and 2025, respectively.
Current wording
Our SG&A expenses ratio was 24.5% and 25.0% for the three months ended September 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 3.1 and 2.8 percentage points on the SG&A expenses ratio for the three months ended September 30, 2026 and 2025. Our SG&A expenses ratio was 25.4% and 25.7% for the first nine months ended September 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 3.4 and 3.0 percentage points on the SG&A expenses ratio for the first nine months ended September 30, 2026 and 2025, respectively.
Previous wording
Excluding the impact of special items, the SG&A expenses ratio decreased by 0.8 and 0.6 percentage points in the second quarter and first six months of 2026, respectively, compared to the prior year periods. The decrease primarily reflects lower headcount, partially offset by annual compensation increases.
Current wording
Excluding the impact of special items, the SG&A expenses ratio decreased by 0.8 and 0.7 percentage points in the third quarter and first nine months of 2026, respectively, compared to the prior year periods. The decrease primarily reflects the benefits of previously implemented cost actions, partially offset by higher accruals under our annual employee incentive compensation plans.
Previous wording
Our R&D expenses ratio was 4.4% and 4.8% for the three months ended June 30, 2026 and 2025, respectively. The special items identified earlier in this section had an unfavorable impact of approximately 0.2 percentage points on the R&D expenses ratio for the three months ended June 30, 2026 and no impact on the R&D expenses ratio for the three months ended June 30, 2025. Our R&D expenses ratio was 4.7% and 5.0% for the first six months ended June 30, 2026 and 2025. The special items identified earlier in this section had an unfavorable impact of approximately 0.3 percentage points on the R&D expenses ratio for the first six months ended June 30, 2026 and no impact on the R&D expenses ratio for the first six months ended June 30, 2025.
Current wording
Our R&D expenses ratio was 4.2% for the three months ended September 30, 2026 and 2025. The special items identified earlier in this section had an unfavorable impact of approximately 0.2 and 0.1 percentage points on the R&D expenses ratio for the three months ended September 30, 2026 and 2025, respectively. Our R&D expenses ratio was 4.6% and 4.7% for the first nine months ended September 30, 2026 and 2025. The special items identified earlier in this section had an unfavorable impact of approximately 0.4 percentage points on the R&D expenses ratio for the first nine months ended September 30, 2026 and no impact on the R&D expenses ratio for the first nine months ended September 30, 2025.
Previous wording
Excluding the impact of special items, the R&D expenses ratio decreased by 0.6 percentage points in the second quarter and first six months of 2026, compared to the prior year periods. The decrease is primarily due to phasing of R&D spend which is expected to be flat on a full year basis.
Current wording
Excluding the impact of special items, the R&D expenses ratio decreased by 0.1 and 0.5 percentage points in the third quarter and first nine months of 2026, respectively, compared to the prior year periods. The decrease is primarily due to the benefits of previously implemented cost actions.
Previous wording
In recent years, we have undertaken actions to transform our cost structure and enhance operational efficiency. These efforts have included restructuring the organization into verticalized segments, optimizing our manufacturing footprint, R&D operations, and supply chain network, employing disciplined cost management, and centralizing and streamlining certain support functions. The related costs of these actions consisted primarily of employee termination costs, implementation costs, contract termination costs, and asset impairments.
Current wording
In recent years, we have undertaken actions to transform our cost structure and enhance operational efficiency. These efforts have included restructuring the organization into verticalized segments, optimizing our manufacturing footprint, R&D operations, and supply chain network, employing disciplined cost management, and centralizing and streamlining certain support functions. The related costs of these actions consisted primarily of employee termination costs, implementation costs, contract termination costs, and asset write offs.
Previous wording
For the six months ended June 30, 2026, $58 million of the restructuring charges, consisting of employee termination costs, were related to initiatives to reduce our cost structure following the sale of our Kidney Care business.
Current wording
For the three and nine months ended September 30, 2026, $21 million and $79 million, respectively, of the restructuring charges, consisting of employee termination costs, were related to initiatives to reduce our cost structure following the sale of our Kidney Care business. For the three and nine months ended September 30, 2026, $39 million of the restructuring charges, consisting of $7 million of contract termination and other costs and $32 million of asset write offs, were related to the cessation of production of certain products at one of our specialty injectables manufacturing facilities.
Previous wording
We currently expect to incur additional pre-tax costs, primarily related to the implementation of business optimization programs, that are not material to our condensed consolidated financial statements, through the completion of certain initiatives that are currently underway. We continue to pursue cost savings initiatives, including those intended to mitigate a portion of the dis-synergies that arose as a result of the sale of our Kidney Care business, and to the extent further cost savings opportunities are identified, we would incur additional restructuring charges and costs to implement business optimization programs in future periods. Refer to Note 10 in Item 1 of this Quarterly Report on Form 10-Q for additional information regarding our business optimization programs.
Current wording
We currently expect to incur additional pre-tax costs, primarily related to the implementation of business optimization programs, that are not material to our condensed consolidated financial statements, through the completion of certain initiatives that are currently underway. We continue to pursue cost savings initiatives, including those intended to mitigate a portion of the dis-synergies that arose as a result of the sale of our Kidney Care business, and to the extent further cost savings opportunities are identified, we would incur additional restructuring charges and costs to implement future business optimization programs in future periods. Refer to Note 10 in Item 1 of this Quarterly Report on Form 10-Q for additional information regarding our business optimization programs.
Previous wording
Other operating income, net was $49 million and $52 million in the second quarter of 2026 and 2025, respectively, and $91 million and $92 million for first six months ended June 30, 2026 and 2025, respectively. These amounts were primarily related to the income recognized under the Kidney Care TSA entered into upon the sale of the Kidney Care business in January 2025.
Current wording
Other operating income, net was $86 million and $48 million in the third quarter of 2026 and 2025, respectively, and $177 million and $140 million for first nine months ended September 30, 2026 and 2025, respectively. These amounts were primarily related to the income recognized under the Kidney Care TSA entered into upon the sale of the Kidney Care business in January 2025. In the third quarter and first nine months of 2026, this amount also included a net benefit from the settlement of certain patent infringement claims.
Previous wording
Interest expense, net was $64 million and $58 million in the second quarter of 2026 and 2025, respectively, and $130 million and $122 million for first six months ended June 30, 2026 and 2025, respectively. The increase in the second quarter and first six months of 2026 was driven by higher interest expense on senior notes issued in the fourth quarter of 2025 partially offset by debt repayments in the first six months of 2025.
Current wording
Interest expense, net was $61 million and $58 million in the third quarter of 2026 and 2025, respectively, and $191 million and $180 million for first nine months ended September 30, 2026 and 2025, respectively. The increase in the third quarter and first nine months of 2026 was driven by higher interest expense on senior notes issued in the fourth quarter of 2025, partially offset by debt repayments in the first nine months of 2026 and 2025.
Showing the first 40 of 71 pairs. Open the source sections for the rest.
Rearranged current paragraphs (2)
Current report — wording carried from elsewhere
Based on the VAI reclassification, Baxter expects that the 2023 Warning Letter will be closed and no additional Warning Letters on the facilities will remain outstanding.
Current report — wording carried from elsewhere
3 Available online at https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/baxter-international-inc-733231-09292026