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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 2201–2220 of 7756 recalls

Baxter Healthcare Corporation: Compella Therapy Air Supply Unit

Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.

FDAFeb 14, 2022Nationwide• Baxter Healthcare Corporation

Baxter Healthcare Corporation: Compella Bariatric Bed System

Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.

FDAFeb 14, 2022Nationwide• Baxter Healthcare Corporation

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: Cytocell 8 Square Template Slides (Glass)- microscope sli...

Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as shown on the outer label.

1...109 110111112 113...388

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FDAFeb 14, 2022Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Norepinephrine Bitartrate (BayCare) – Subpotent Drug (2022)

Subpotent drug

Class IIILow

FDAFeb 14, 2022FL• BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy

Perfect Sleeper Mattresses (Serta) – Flammability Risk (2022)

Fire/Burn Risk

This recall involves Serta Perfect Sleeper-branded mattresses. The white single-sided mattresses have navy blue side panels and were sold in twin, twin XL, full, queen, king and California king sizes. They were manufactured from July 15, 2021 through August 6, 2021. The date of manufacture in DD/MM/YY, the model number and "Prototype ID: L1" can be found on a white tag sewn into the head of the mattress. The following model numbers are included in this recall: 500102413 500105863 500108763 500702313 500102513 500106563 500109563 500952763 500102863 500106663 500302913 500953063 500102963 500106763 500304013 500960143 500103063 500107263 500701113 500960243 500103163 500107463 500702013 500960443 500702313

CPSCFeb 10, 2022Nationwide• SSB Manufacturing Company, of Doraville, Ga.

Bio-Rad Laboratories, Inc.: BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RP...

Due to current concerns related to COVID-19 vaccine interference with the RPR portion of the BioPlex 2200 Syphilis Total & RPR panel, as well as intermittent manufacturing challenges to produce RPR reagents that consistently meet stability specifications

FDAFeb 8, 2022Nationwide• Bio-Rad Laboratories, Inc.

Bio-Rad Laboratories, Inc.: BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator...

FDAFeb 8, 2022Nationwide• Bio-Rad Laboratories, Inc.

RED MAMMOTH Capsules (Celebrate Today) – Undeclared Ingredients (2022)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Class IHigh

FDAFeb 8, 2022Nationwide• Celebrate Today

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: TCL1 Breakapart Probe, Fluorescence in situ hybridisation...

May show unexpected locus specific signals in addition to those at 14q32.

FDAFeb 4, 2022MN• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Prevantics Maxi Swabstick (PDI) – Manufacturing Method Uncertainty (2022)

cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.

Class IIModerate

FDAFeb 4, 2022Nationwide• Professional Disposables International, Inc.

Prevantics Swabstick (PDI) – Manufacturing Method Uncertainty (2022)

cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.

Class IIModerate

FDAFeb 4, 2022Nationwide• Professional Disposables International, Inc.

Prevantics Swab (PDI) – Manufacturing Method Uncertainty (2022)

cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.

Class IIModerate

FDAFeb 4, 2022Nationwide• Professional Disposables International, Inc.

Abbott Laboratories, Inc: Alinity s System software version2.8.0, REF LN 06P16-01, ...

Software error associated with the immunoassay analyzer wash cycle which is using 1 mL of wash buffer instead of the intended 3 mL of wash buffer to wash the exterior of the probe.

FDAFeb 3, 2022Nationwide• Abbott Laboratories, Inc