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Baxter Healthcare Corporation

Baxter Healthcare Corporation Recalls

All product recalls associated with Baxter Healthcare Corporation.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 501–520 of 7756 recalls

Progressa Bed Surfaces (Baxter) – Air Bladder Movement (2025)

The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

TruSystem 7500 Stationary Column (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

TruSystem 7500 Hybrid (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

FDA

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Page 26 of 388Next

Feb 25, 2025

Nationwide

• Baxter Healthcare Corporation

TruSystem 7500 Hybrid (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

DR Field and Brush Mower – Laceration Risk (2025)

Laceration Risk

This recall involves DR Power Tow Behind Field and Brush Mowers. The black and orange tow behind mowers have the following model and serial numbers, printed on a white label that is on the front frame of the mower. "DR" is printed on the front of the mowers. Only mowers manufactured between April 1, 2024, and August 20, 2024, are included in this recall. The manufacture date is on the serial number label affixed to the rear frame of the unit and is listed in YYYYMMDD format. Model Description Serial No. Range TB21044BEN DR BRUSH MOWER PREMIER 44T 10.5 HP BS ES 3014835626 to 3015507481 TB23244BEN DR BRUSH MOWER PRO 44T 17.5 HP BS ES 3014860338 to 3015403241 TB25344BEN DR BRUSH MOWER PRO XL44T 20 HP BS ES 3014916847 to 3015451110 TB27052BEN DR BRUSH MOWER PRO MAX52T 22 HP BS ES 3014839204 to 3015534243

CPSCFeb 20, 2025Nationwide• DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin

Avastin Intravitreal Injection (Turbare) – Sterility Concern (2025)

Lack of Assurance of Sterility: due to a quality control process deviation. During an internal quality assurance review, an Acceptable Quality Limit (AQL) inspection was not conducted on a statistically sound number of samples. This may result in the inability to assure that the impacted products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess and may lead to products of unacceptable quality.

Class IIModerate

FDAFeb 18, 2025Nationwide• Turbare Manufacturing