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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

566

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 1161–1180 of 7756 recalls

Dianeal Low Calcium Solution (Baxter) – sterility concern (2023)

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Class IIModerate

FDAAug 11, 2023Nationwide• Baxter Healthcare Corporation

Functional MR Software (Olea Medical) – Export Error (2023)

When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file contents and associated series descriptions to not match, which could lead to a misinterpretation of clinical data.

FDAAug 10, 2023MA, MI• OLEA MEDICAL 93 AVANUE DU SORBIER, ZONE ATHELIA IV LA CIOTAT France

Epiphany Cardio Server (Baxter) – Software Correction (2023)

Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical Device Correction for the Cardio Server E3 ECG Management System software listed below due to a report of the caliper tool becoming non-responsive, preventing the caliper function from being used temporarily on software versions v6.1.x, v6.2.x, and v7.0.x of the E3 user interface.

1...57 585960 61...388

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FDAAug 10, 2023Nationwide• Baxter Healthcare Corporation

Welch Allyn Connex Monitor (Baxter) – Display Tape Placement (2023)

Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.

FDAAug 10, 2023Nationwide• Baxter Healthcare Corporation

Oculus Myopia Master (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Oculus Pentacam AXL Wave (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Oculus Pentacam AXL (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Liquid Assayed Chemistry Control (Randox) – instructions error (2023)

there has been a transcription error in the Instructions for Use (IFU) for the Liquid Assayed Chemistry Control Premium Plus Level 3. For Caeruloplasmin, the one and two standard deviation values printed on the sheet are incorrect, which may lead to misreporting patient results. Target and range values are correct, and risk is mitigated; most clinical labs will use the target and range values in clinical practice.

FDAAug 3, 2023GA, OH, OR +3 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Helix CBD Clinical Cream (Parker Labs) – CGMP Manufacturing Issues (2023)

CGMP Deviations

Class IIModerate

FDAAug 2, 2023Nationwide• Parker Laboratories, Inc.

Helix Pain Relief Cream (Parker Labs) – CGMP Manufacturing Issues (2023)

CGMP Deviations

Class IIModerate

FDAAug 2, 2023Nationwide• Parker Laboratories, Inc.

Protex Hand Sanitizer (Parker Labs) – CGMP Manufacturing Issues (2023)

CGMP Deviations

Class IIModerate

FDAAug 2, 2023Nationwide• Parker Laboratories, Inc.

Helix Tri-Active Therapy Cream (Parker Labs) – CGMP Manufacturing Issues (2023)

CGMP Deviations

Class IIModerate

FDAAug 2, 2023Nationwide• Parker Laboratories, Inc.

Helix CBD Therapy Cream (Parker Labs) – CGMP Manufacturing Issues (2023)

CGMP Deviations

Class IIModerate

FDAAug 2, 2023Nationwide• Parker Laboratories, Inc.

Caesar Salad Kit (Fresh Creative) – Deer feces risk (2023)

Product potentially contaminated with deer feces

Class IIModerate

FDAAug 2, 2023IL, IN• RMJV, LP dba Fresh Creative Foods

Spring Water Jugs (Ruby Mountain) – Coliform Contamination (2023)

Firm's sample revealed positive findings for coliforms.

Class IIILow

FDAAug 1, 2023NV• RUBY MOUNTAIN SPRING WATER

Ford Transit (FARBER SPECIALTY) – fuel hose issue (2023)

Fire/Burn Risk

Farber Specialty Vehicles (Farber) is recalling one 2021 Ford Transit van equipped with a Cummins Onan QG 2800i generator. The fuel hose between the inline fuel filter and the Injection Pump Module (IPM) may have inadequate clamp force, possibly resulting in a gasoline leak.

NHTSAJul 31, 2023Nationwide• FARBER SPECIALTY

Guider Softip Guide Catheter 8F (Boston Scientific) – tip curve issue (2023)

Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.

FDAJul 27, 2023Nationwide• Boston Scientific Corporation

Guider Softip Guide Catheter 6F (Boston Scientific) – tip curve issue (2023)

FDAJul 27, 2023Nationwide• Boston Scientific Corporation

Guider Softip Guide Catheter 5F (Boston Scientific) – tip curve issue (2023)

FDAJul 27, 2023Nationwide• Boston Scientific Corporation

Tobramycin Ophthalmic Solution (Alembic) – Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJul 27, 2023Nationwide• ALEMBIC PHARMACEUTICALS, INC.