Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 661680 of 56,506 recalls

Medical DeviceNovember 24, 2025· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Sensor UDI-DI code: 00357599818005 The Recalled by Abbott...

The Issue: Due to a manufacturing process issue that may cause carbon build up in the...

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

Class I — Serious Health HazardOngoing
DrugNovember 24, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 24, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 24, 2025· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599844011 Recalled by Abbott...

The Issue: Due to a manufacturing process issue that may cause carbon build up in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2025· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599843014 Recalled by Abbott...

The Issue: Due to a manufacturing process issue that may cause carbon build up in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2025· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599819002 Recalled by Abbott...

The Issue: Due to a manufacturing process issue that may cause carbon build up in the...

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: 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
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Vivoo Vaginal pH Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd....

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: The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips 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 pH Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd. Due to...

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