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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 5881–5900 of 37665 recalls

GEM Flow Coupler Monitor (Baxter) – Display Channel Error (2023)

An issue was identified where the LCD monitor display may not indicate the correct active channel. The issue occurs when the monitor is turned on using battery power, and channel B was selected as the last active channel prior to powering down.

Moderate

FDAJun 19, 2023Nationwide• Baxter Healthcare Corporation

ProPlan CMF Guide (Materialise) – Incorrect Guide Versions (2023)

Wrong versions of guides 3A and 3B (Patient Specific) were shipped prior to the re-design request

Moderate

FDAJun 19, 2023Nationwide• Materialise N.V. Technologielaan 15 Heverlee Belgium

TESLA MODEL Y (Tesla) – Battery Disconnect Defect (2023)

Tesla, Inc. (Tesla) is recalling certain 2023 Model 3 and Model Y vehicles. The pyrotechnic battery disconnect may be defective.

High

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NHTSA

Jun 19, 2023

Nationwide

• TESLA

ALTEC L SERIES Aerial Device (Altec) – Hydraulic Hose Installation (2023)

Altec Industries, Inc. (Altec) is recalling certain 1999-2022 L Series and LR Series aerial devices. A hydraulic hose may have been installed between the cylinder port and load-holding valve instead of metallic tubing, which can result in a damaged hydraulic hose and failure of the load-holding feature.

Moderate

NHTSAJun 16, 2023Nationwide• ALTEC

Tramadol Hydrochloride Tablets (Harvard Drug) – Packaging Defect (2023)

Packaging defect: blister packaging inadequately sealed.

Class IIModerate

FDAJun 16, 2023Nationwide• The Harvard Drug Group

Tostitos Avocado Salsa (Frito-Lay) – Undeclared Milk (2023)

Undeclared Milk

Undeclared milk

Class IHigh

FDAJun 16, 2023Nationwide• Frito-Lay, Inc. Headquarters

HAMILTON C2 Ventilator (Hamilton Medical) – Software Anomaly (2023)

Due to a software anomaly after approximately 91 days of cumulative use, the ventilator may stop and enter the ambient mode without prior notice.

Moderate

FDAJun 15, 2023AL, AK, AZ +47 more• Hamilton Medical, Inc.

HAMILTON T1 Ventilator (Hamilton Medical) – Software Anomaly (2023)

Due to a software anomaly after approximately 91 days of cumulative use, the ventilator may stop and enter the ambient mode without prior notice.

Moderate

FDAJun 15, 2023AL, AK, AZ +47 more• Hamilton Medical, Inc.

Spectrum IQ Infusion System (Baxter) – Device Correction (2023)

A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Software infusion pumps due to an increase in reported false upstream occlusion alarms following upgrades to software versions v8.01.01 and v9.02.01.

Moderate

FDAJun 15, 2023Nationwide• Baxter Healthcare Corporation

HAMILTON C3 Ventilator (Hamilton Medical) – Software Anomaly (2023)

Due to a software anomaly after approximately 91 days of cumulative use, the ventilator may stop and enter the ambient mode without prior notice.

Moderate

FDAJun 15, 2023AL, AK, AZ +47 more• Hamilton Medical, Inc.

SIGMA Spectrum Infusion Pump (Baxter) – Device Correction (2023)

Moderate

FDAJun 15, 2023Nationwide• Baxter Healthcare Corporation

HAMILTON C1 Ventilator (Hamilton Medical) – Software Anomaly (2023)

Due to a software anomaly after approximately 91 days of cumulative use, the ventilator may stop and enter the ambient mode without prior notice.

Moderate

FDAJun 15, 2023AL, AK, AZ +47 more• Hamilton Medical, Inc.

Promax Hydraulic Disc Brakes (Trek) – Crash Hazard (2023)

This recall involves Trek bicycles with revision 1 of the Promax Solve DSK-925 and Promax F1 DSK-927 hydraulic disc brakes installed as original equipment on the bicycle models listed in the table below. The serial number is printed on a sticker underneath the frame of the bicycle. Trek Bicycles Model Year 21: FX 2, Verve 3, Verve+ 3. Trek Bicycles Model Year 22: FX2, FX 3, Verve 3, Verve+ 3, FX Sport 4, FX Sport 5, FX Sport 6, Dual Sport 2, Dual Sport 3. Trek Bicycles Model Year 23: FX2, FX3, FX Sport 4, FX Sport 5, FX Sport 6, Dual Sport + 2, FX + 2.

Moderate

CPSCJun 15, 2023Nationwide• Lee Chi Enterprises Co., Ltd.

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

GREAT DANE EVEREST (Great Dane) – Tire Pressure Monitoring Issue (2023)

Great Dane Trailers (Great Dane) is recalling certain 2024 Champion and Everest dry van trailers equipped with Tire Pilot Plus-Electronic Regulator Control Unit assemblies. All 8 tires may experience a loss of tire pressure while driving faster than 45 mph.

Moderate

NHTSAJun 14, 2023Nationwide• GREAT DANE

IntelliVue Patient Monitor (Philips) – ECG Capability Configuration (2023)

Devices with Option CP2 and initially programmed to software version P.01.01 were configured incorrectly at the factory. Therefore, Enhanced ECG Capabilities provided by Option CP2 were not enabled in these devices. Without Option C01 Full Arrhythmia, the device will not provide the yellow alarms for enhanced arrhythmia detection. This is a retrospectively reported recall from 6/14/23.

Moderate

FDAJun 14, 2023Nationwide• Philips North America Llc

TESLA SEMI (Tesla) – Door Warning Indicator Issue (2023)

Tesla, Inc. (Tesla) is recalling certain 2023 Semi vehicles. The door open warning indicator only displays when the vehicle's parking brake is not engaged and the side door is not fully latched. In addition, the door closure warning system allows the operator to dismiss the notification that the side door is unlatched, which could result in driving with an unsecured door. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 206, "Door Locks and Door Retention Components."

Moderate

NHTSAJun 13, 2023Nationwide• TESLA

PETERBILT 579 (Peterbilt) – Electrical System Fastener Problem (2023)

Fire/Burn Risk

PACCAR, Incorporated (PACCAR) is recalling certain 2021-2023 Peterbilt 579 vehicles equipped with MX-13 engines and 160-amp alternators. A fastener on the front spring bracket may have been installed with the head on the outside of the frame rail, which can chafe and damage the alternator positive cable.

High

NHTSAJun 13, 2023Nationwide• PETERBILT

Stryker Infinity Alignment Frame (Wright Medical) – Pin Sleeve Hole Defect (2023)

The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.

Moderate

FDAJun 13, 2023Nationwide• Wright Medical Technology, Inc.