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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

593

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 921–940 of 10391 recalls

Braun Thermoscan PRO 6000 (Baxter) - Outdated Instructions (2024)

The Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).

Low

FDAJun 13, 2024Nationwide• Baxter Healthcare Corporation

Amana, Daikin, Goodman Air Conditioning Units – manufacturing defect (2024)

Fire/Burn Risk

This recall involves Amana, Daikin, and Goodman branded packaged air conditioners and heat pumps. The recalled units are gray or green in color, and can be identified by the model number located on the electrical connection side of the unit on the outside panel. To see if your product is subject to this recall, visit www.goodmanmfg.com/package-recall.

High

CPSCJun 13, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas

Yellowfin Tuna Loin (Fresh Catch) – High histamine levels (2024)

1...45 464748 49...520

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High histamine levels in Yellowfin Tuna

Class IIModerate

FDAJun 12, 2024CA• Fresh Catch Inc

SURGICEL Fibrillar (Ethicon) - Packaging Integrity (2024)

Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.

Moderate

FDAJun 11, 2024Nationwide• Ethicon Sarl, a Johnson & Johnson Company rue du Puits-Godet 20 Neuchatel Switzerland

Thor Motor Coach Tranquility (Thor) - Circuit Breaker (2024)

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain 2025 Thor Tranquility and Sanctuary motorhomes. A 50 AMP circuit breaker was incorrectly installed when a 20 AMP breaker is required, which can result in overheated wiring.

High

NHTSAJun 11, 2024Nationwide• THOR MOTOR COACH

Thor Motor Coach Indigo (Thor) - Heat Shield (2024)

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain 2024-2025 Indigo and Luminate motorhomes. The heat shield that protects the propane tank from engine exhaust may be too short, which can cause the propane tank to become overheated.

High

NHTSAJun 11, 2024Nationwide• THOR MOTOR COACH

OMTech Desktop Laser Engraver (Rygel Advanced Machines) – Interlocks Missing (2024)

Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.

Low

FDAJun 7, 2024Nationwide• Rygel Advanced Machines d/b/a Omtech Laser

Philips SENSE XL Torso Coil (Philips) – Patient Burn Risk (2024)

Fire/Burn Risk

Potential for coils to heat up and harm patients (burn).

Moderate

FDAJun 5, 2024Nationwide• Philips North America Llc

Philips SENSE XL Torso Coil Mk2 (Philips) – Patient Burn Risk (2024)

Fire/Burn Risk

Potential for coils to heat up and harm patients (burn).

FDAJun 5, 2024Nationwide• Philips North America Llc

Philips SENSE XL Torso Coil (Philips) – Patient Burn Risk (2024)

Fire/Burn Risk

Potential for coils to heat up and harm patients (burn).

FDAJun 5, 2024Nationwide• Philips North America Llc

Trulight 5000/3000 Surgical Light (Baxter) – Thermal Injury Risk (2024)

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads

FDAJun 4, 2024Nationwide• Baxter Healthcare Corporation

VidiaPort Carrying Arm (Baxter) – Thermal Injury Risk (2024)

FDAJun 4, 2024Nationwide• Baxter Healthcare Corporation

iLED 7 Surgical Lights (Baxter) – Thermal Injury Risk (2024)

FDAJun 4, 2024Nationwide• Baxter Healthcare Corporation

Welch Allyn CP150 Electrocardiograph (Baxter) – EMI Absorber Missing (2024)

During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the vicinity or the device itself may be vulnerable to EMI resulting in device malfunction or unavailability.

FDAJun 3, 2024IL• Baxter Healthcare Corporation

Oshkosh S-Series Steering Gear (Oshkosh) – Replacement Part Defect (2024)

Oshkosh Corporation (Oshkosh) is recalling certain Shepphard Steering Gears, with part number 3875726, sold as replacement parts for certain S-Series vehicles. The steering gears may have been assembled incorrectly, which can cause the gear to fracture.

NHTSAMay 31, 2024Nationwide• OSHKOSH

Homeopathic Kit (Washington Homeopathic) – Labeling Mix-up (2024)

Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.

Class IIILow

FDAMay 31, 2024Nationwide• Washington Homeopathic Products, Inc.

Volara System Circuit (Baxter) – Handset Plug Disconnect (2024)

Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.

FDAMay 30, 2024Nationwide• Baxter Healthcare Corporation

Volara System Blue Ventilator Adapter (Baxter Healthcare) – Disconnection Risk (2024)

Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.

FDAMay 30, 2024Nationwide• Baxter Healthcare Corporation

Life2000 Ventilator (Baxter Healthcare) – Battery Charging Failure (2024)

Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behavior due to damage to the battery charger dongle. Damage of the battery charger dongle prevents the ventilator's internal battery from charging.

FDAMay 29, 2024Nationwide• Baxter Healthcare Corporation

Presource Kits (Cardinal Health) – FDA Disposition Concern (2024)

Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical supplied finished kits. Merit Medical supplied finished kits are included as components in Presource kits. According to the FDA s communication, these Shenli syringes, located inside a Merit Medical kit component, cannot be distributed for use as they could contain a significant change or modification in design which could significantly alter the safety or effectiveness of the finished kit product, resulting in the risk of patient harm such as inaccurate dosing and a leaking device.

FDAMay 29, 2024Nationwide• Cardinal Health 200, LLC