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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

589

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 4381–4400 of 10393 recalls

Gambro Low Volume Blood System (Baxter) – Tubing Disconnection (2020)

Potential disconnection of tubing set.

Moderate

FDAApr 17, 2020Nationwide• Baxter Healthcare Corporation

Flounder Stuffed Seafood (Freedman) – undeclared milk (2020)

Undeclared Milk

Product may contain undeclared Milk (whey listed in ingredients)

Class IIModerate

FDAApr 17, 2020TX• Freedman Food Service, Inc dba Buckhead Meat & Seafood of Houston

Flounder Stuffed Seafood (Freedman) – multiple allergens (2020)

Undeclared Gluten

Product may contain undeclared Wheat, Soy, Eggs, and Milk

1...218 219220221 222...520

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Class I

High

FDAApr 17, 2020TX• Freedman Food Service, Inc dba Buckhead Meat & Seafood of Houston

Energy Formula Multivitamins (Vitamin Shoppe) – packaging safety (2020)

This recall involves The Vitamin Shoppe's Energy Formula multivitamins in a white bottle with a blue, white, and gold label. Each bottle contains 90 tablets and has the code VS-3293 with the lot number 8102351 located on the bottom of the bottle.

Low

CPSCApr 16, 2020Nationwide• The Vitamin Shoppe, of Secaucus, N.J.

Advanced Joint Relief Capsules (Absorb Health) – allergen warning (2020)

The firm was notified by the FDA that they failed to included a shellfish allergen on their ingredient panel.

Class IIModerate

FDAApr 15, 2020AZ, CA, FL +14 more• Absorb Health LLC

Acetaminophen Codeine Tablet (Pharma Pac) – Quality Deviation (2020)

cGMP Deviations

Class IIModerate

FDAApr 15, 2020AZ, CA, IN• H J Harkins Company Inc dba Pharma Pac

Cardiovascular Monitoring Device (Philips) – Latex Warning (2020)

The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex.

FDAApr 13, 2020Nationwide• Philips North America, LLC

MRI Diagnostic Device (Philips) – Latex Warning (2020)

The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex.

FDAApr 13, 2020Nationwide• Philips North America, LLC

IPS e.max ZirCAD (Ivoclar Vivadent) – Cracking Risk (2020)

Restorations crack during the sintering process.

FDAApr 13, 2020Nationwide• Ivoclar Vivadent AG Benderer Strasse 2 Schaan Liechtenstein

HeartStart XL Defibrillator (Philips) – Switch Failure (2020)

The rotary therapy selector switch may fail, resulting in unexpected device behavior including: 1) The device may not turn on; 2) The device may not perform the selected function;3) The device may deliver a shock with an energy level different than the setting selected by the user. In any of these scenarios, appropriate therapy delivery may be delayed.

FDAApr 13, 2020Nationwide• Philips North America, LLC

Zenition 50 X-Ray System (Philips) – Cable Strain (2020)

When strain relief is lost at the stand side of the Stand MVS Trolley Cable, over time one or more electrical contacts could break due to pulling, twisting, or dropping of the connector. If this happens, live parts may be exposed (230 V) and/or the video signal can be lost.

FDAApr 10, 2020Nationwide• Philips North America, LLC