Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,710 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,710 in last 12 months

Showing 421440 of 29,188 recalls

Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2025· Ferndale Laboratories, Inc.

Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...

The Issue: Butyrate tube cracks during actuation, rendering product unusable.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2025· ICU Medical, Inc.

Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...

The Issue: For certain customers, the Change Summary review option ceases to operate as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2025· Draeger, Inc.

Recalled Item: Draeger Vapor 2000. Unheated Recalled by Draeger, Inc. Due to A certain...

The Issue: A certain component of affected devices was not delivered within...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2025· ICU Medical, Inc.

Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...

The Issue: Software issue only allows Concentration Limits to be defined to one digit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to...

The Issue: Ophthalmic procedure packs may have incomplete seals affecting sterility.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2025· Draeger, Inc.

Recalled Item: Draeger Vapor 3000. Unheated Recalled by Draeger, Inc. Due to A certain...

The Issue: A certain component of affected devices was not delivered within...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2025· Smith & Nephew, Inc.

Recalled Item: BIOSURE HA SCREW Recalled by Smith & Nephew, Inc. Due to Removal of affected...

The Issue: Removal of affected lot of screws due to labeling error.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: S. Typhi/Para Typhi A Antigen Recalled by Changchun Wancheng Bio-Electron...

The Issue: Test strips and other tests including for near-patient testing, that require...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Male Fertility Sperm Test for Home Use (Cassette) Recalled by Changchun...

The Issue: Test strips and other tests including for near-patient testing, that require...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Exploro Highly Sensitive Male Fertility / Sperm Concentration Test Recalled...

The Issue: Test strips and other tests including for near-patient testing, that require...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Vivoo Protein Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd. Due...

The Issue: Test strips and other tests including for near-patient testing, that require...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: LotFancy Urinary Tract Infection Urine (UTI) Test Strips Recalled by...

The Issue: Test strips and other tests including for near-patient testing, that require...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing