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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

1000

Class I (Serious)

143

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 4541–4560 of 37665 recalls

Baxter Exactamix Pro (Baxter) – overfill software error (2023)

An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.

High

FDADec 22, 2023AL, AZ, CA +19 more• Baxter Healthcare Corporation

Aligned Lower Extremity Pack (Windstone) – saline sterility issue (2023)

Sterility assurance for saline included in surgical kits cannot be guaranteed.

Low

FDADec 22, 2023CA, FL, IL• Windstone Medical Packaging, Inc.

GE Voluson Probe (GE Healthcare) – image artifact risk (2023)

GE HealthCare has become aware of an issue with certain IC9-RS ultrasound probes (see Affected Products List) that can result in a double image artifact creating a ghost image with realistic features. An unrecognized artifact may lead to misdiagnosis.

High

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Page 228 of 1884Next

FDA

Dec 22, 2023

Nationwide

• GE HEALTHCARE AUSTRIA GMBH & CO Tiefenbach 15 Pfaffing Austria

HRIS ACET Cup (Howmedica) – seal integrity failure (2023)

Failed to meet the acceptance criteria for the seal integrity and/or package integrity testing for the Sterile Barrier Outer Pouch and the Protective Barrier Inner Pouch, compromising product sterility

Low

FDADec 22, 2023Nationwide• Howmedica Osteonics Corp.

Freightliner M2 (Freightliner) – transmission indication fault (2023)

Daimler Trucks North America, LLC (DTNA) is recalling certain 2024 Freightliner M2 Business Class vehicles. The vehicle may be incorrectly equipped with a transmission gear shifter that includes a 'PARK' position despite the transmission not having a park pawl.

High

NHTSADec 22, 2023Nationwide• FREIGHTLINER

Solgar Glucosamine Chondroitin (Nestle) – packaging error (2023)

Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.

Class IIILow

FDADec 22, 2023IN, NV, NY +3 more• Nestle Product Technology Center - Nestle Health Science

Baxter Exactamix Pro (Baxter) – overfill software error (2023)

High

FDADec 22, 2023AL, AZ, CA +19 more• Baxter Healthcare Corporation

Melissa's Hot Kimchi (World Variety) – undeclared fish (2023)

Undeclared Allergen

Undeclared allergen; fish.

Class IHigh

FDADec 22, 2023CA, FL, TX• World Variety Produce Inc dba Melissa's

Henry Schein Masks (AMD Medicom) – production equipment problem (2023)

Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products.

Low

FDADec 21, 2023Nationwide• AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada

Medline Blood Culture Bottle Kit (Medline) – kit quality issue (2023)

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.

Low

FDADec 21, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Henry Schein Masks (AMD Medicom) – production equipment problem (2023)

Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products.

Low

FDADec 21, 2023Nationwide• AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada

Pella Architect Series Windows – injury risk (2023)

This recall involves Pella's Architect Series venting wood and aluminum-clad casement windows. The following four custom-made casement window types are included in this recall: all venting hurricane impact products with side pivot hardware, all venting casements with a frame height greater than 96 inches, all venting casements with a frame width wider than 35 inches, and all venting casements with a frame width greater than 29 inches and a vent height greater than 47 inches with side pivot hardware. The serial number is etched in a lower corner of the window glass. Serial numbers included in this recall can be verified at www.PellaHingeRecall.expertinquiry.com.

Moderate

CPSCDec 21, 2023Nationwide• Pella Corporation, of Pella, Iowa

Freightliner Sprinter 4500 (Freightliner) – propeller connection fault (2023)

Fire/Burn Risk

Daimler Vans USA, LLC (DVUSA) is recalling certain 2020 Mercedes-Benz Sprinter and Freightliner Sprinter vehicles. The connection between the propeller shaft bearing and crossmember may loosen, reducing vehicle control.

High

NHTSADec 21, 2023Nationwide• FREIGHTLINER

Patterson Procedure Masks (AMD Medicom) – production equipment problem (2023)

Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products.

Low

FDADec 21, 2023Nationwide• AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada

Freightliner Sprinter 3500 (Freightliner) – frame member issue (2023)

Daimler Vans USA, LLC (DVUSA) is recalling certain 2019-2021 Mercedes-Benz Sprinter and Freightliner Sprinter vehicles. The longitudinal frame members may be missing reinforcement fasteners, reducing vehicle stability and decreasing the structural integrity of the third-row seats.

High

NHTSADec 21, 2023Nationwide• FREIGHTLINER