Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Baxter Healthcare Corporation

Baxter Healthcare Corporation Recalls

All product recalls associated with Baxter Healthcare Corporation.

Get alerts for this brand

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 3201–3220 of 37665 recalls

Baxter Spectrum Wireless Battery Modules A/B/G/N, (Baxter Healthcare Corporation) – the spectrum wbm may fail to auto-doc... (2024)

The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.

High

FDAJul 17, 2024Nationwide• Baxter Healthcare Corporation

Spectrum Wireless Battery Modules A/B/G/N, (Baxter Healthcare Corporation) – the spectrum wbm may fail to auto-doc... (2024)

Moderate

FDAJul 17, 2024Nationwide• Baxter Healthcare Corporation

WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC... (Boston Scientific Neuromodulation Corporation) – spinal cord stimulation (scs) implant... (2024)

1...159 160161162 163...1884

Page 161 of 1884Next

Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset, which may lead to transient loss of stimulation; patients may experience undesired sensations when therapy turns off for approx. 10-15 seconds and then back on, which may lead patient to request surgical intervention for replacement or revision.

High

FDAJul 17, 2024Nationwide• Boston Scientific Neuromodulation Corporation

CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160... (Smiths Medical ASD Inc.) – damage to the battery pack may have c... (2024)

Damage to the battery pack may have caused a short to a capacitor within the battery pack. While the battery encasement is designed to be flame retardant, a short to the capacitor could lead to melting of the battery pack case. If this issue occurs, the battery pack charging circuit may become inoperable.

High

FDAJul 16, 2024Nationwide• Smiths Medical ASD Inc.

2024 TRIPLE E RV WONDER – fall hazard (2024)

Triple E Recreational Vehicles (Triple E) is recalling certain 2020-2024 Wonder W24RL, W24FTB, W24MBL, and W24MB motorhomes. The floor structure to the crossmember may be inadequately secured, causing the generator to fall.

High

NHTSAJul 16, 2024Nationwide• TRIPLE E RV

Beckman Coulter IRISPEC CA/CB/CC Urine Chemistry Controls... (Beckman Coulter, Inc.) – beckman coulter has become aware of a... (2024)

Beckman Coulter has become aware of an increase in customer complaints for intermittent IRISpec CB negative glucose control failure, resulting in false positive control results when used in conjunction with iChemVELOCITY Urine Chemistry Strips (PNs 800-7204 and 800-7212) on the iChemVELOCITY Analyzer. This issue may delay the reporting of patient results, with a worst-case scenario of a delay in diagnosis or treatment of metabolic disorders, kidney function abnormalities, urinary tract infections, and liver function.

Moderate

FDAJul 16, 2024Nationwide• Beckman Coulter, Inc.

Philips Azurion Interventional Fluoroscopic X-ray System ... (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands) – potential loss of imaging (x-ray) fun... (2024)

Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to Perform Cold Restart

Moderate

FDAJul 15, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Collagen Joint Support (Quantum Fulfillment) – Undeclared Fish (2024)

Undeclared Allergen

Undeclared Fish Allergen

Class IIModerate

FDAJul 15, 2024Nationwide• Quantum Fulfillment and Support, LLC

Aisys (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

Ion Endoluminal System (Intuitive Surgical) – Arm Screw Risk (2024)

There is a potential that the robotic system's instrument cart arm may contain screws that may potentially fail which could result in uncontrolled motion of a catheter inside a patient's airways.

High

FDAJul 12, 2024Nationwide• Intuitive Surgical, Inc.

Avance CS2 (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

ACGO Conversion Kit (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

Salem Travel Trailer (Forest River) – Mislabeled Placard (2024)

Forest River, Inc. (Forest River) is recalling certain 2024 Forest River Salem, Wildwood, and Stealth EVO travel trailers. The Federal Placard may state an incorrect rim size. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims."

High

NHTSAJul 12, 2024Nationwide• FOREST RIVER

DxI 9000 Analyzer (Beckman Coulter) – Electric Short Risk (2024)

Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.

High

FDAJul 12, 2024Nationwide• Beckman Coulter, Inc.

Aespire 100 (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

Amingo (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

Puma Travel Trailer (Forest River) – Trailer Hitch Issue (2024)

Forest River, Inc. (Forest River) is recalling certain 2024 Salem, Puma, Wildwood, and 2025 Cherokee travel trailers equipped with certain Pacific Rim brand couplers. The couplers have an incorrect load rating of 14,000 pounds and may be overloaded, causing the hitch to fail.

High

NHTSAJul 12, 2024Nationwide• FOREST RIVER

Proteus XR/a X-Ray System (GE Healthcare) – Missing Manual (2024)

The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install.

Moderate

FDAJul 12, 2024Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

Aespire 7100 (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.

Aespire 7900 (Datex-Ohmeda) – Gas Outlet Risk (2024)

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Moderate

FDAJul 12, 2024Nationwide• Datex-Ohmeda, Inc.