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Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt. Recalls

All product recalls associated with Baxter Healthcare Corp. Rt..

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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 7161–7180 of 7756 recalls

Baxter Healthcare Corp. Rt.: Baxter''s Patient Care System (BPCS) software, composed o...

If a pharmacy end user alters the Administration Unit of Measure (AUOM) of an ordered drug, the AUOM will display incorrectly on the Medication Administration Record for the patient, possibly leading to medication errors.

FDAJun 16, 2005CA, MA, MO +1 more• Baxter Healthcare Corp. Rt.

Baxter Healthcare Renal Div: Baxter Arena Hemodialysis Systems, product codes ARENADPX...

Operator's Manuals addenda are being issued to provide correct information concerning the correct syringe size to use for heparin infusion, the use of chemical disinfectants in the System 1000, TMP Advise, and Bicarbonate Value calculations.

FDAJun 14, 2005Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Renal Div: Baxter System 1000 Single Patient Hemodialysis Systems, p...

1...357 358359360 361...388

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FDAJun 14, 2005Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Corp. Rt.: Baxter 6060E Epidural Infusion Pump, product code 2L9351 ...

There is an overinfusion condition in the Intermittent mode where the pump may continue to deliver at the higher dose rate instead of switching to the lower keep open rate once the first dose is completed.

FDAJun 13, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter 6060 Multi-Therapy Infusion Pump, product code 2M9...

FDAJun 13, 2005Nationwide• Baxter Healthcare Corp. Rt.

Bunn Home Coffeemakers – electrical issue (2005)

Fire/Burn Risk

The recall involves Bunn® home coffeemakers with model numbers GR-10B, GR-10W, B-10B, B-10W, and BT-10B (including any of those same model numbers ending in the additional letter D) with six-digit date codes ending in "01," "02," or "03." Also involved in the recall are the same models with dates codes ending in "04" and middle digits between "01" and "21." (If the date code has a seventh digit, consumers should ignore the last digit and use the first six digits.) The model number and date code are stamped on a small white or silver sticker on the bottom of the coffeemaker. The 10-cup Bunn® coffeemakers have either a black or white plastic base and top, and measure 14¼ inches high by 7 inches wide by 13¾ inches deep. The word "BUNN®" is printed on the front of the machine in chrome.

CPSCJun 10, 2005Nationwide• Bunn-O-Matic Corp., of Springfield, Ill.

Del Laboratories Inc.: Orajel toddler EXTRA GENTLE Yellow Manual Toothbrush, Mod...

Choking Hazard

Firm received several consumer complaints that the elastomer head of the toothbrush had separated (broke) from the handle during use and could pose a choking hazard to children.

FDAJun 9, 2005Nationwide• Del Laboratories Inc.

Boston Scientific Corporation: Vaxcel Plastic Low Profile Port (non-valved) chest port...

Potential for port housing separation after implantation.

FDAJun 8, 2005Nationwide• Boston Scientific Corporation