Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,848 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,848 in last 12 months

Showing 33613380 of 53,829 recalls

FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Trader Joe's branded Solid White Albacore Tuna in Water Recalled by Chicken...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Van Camp's branded Solid Light Yellowfin in Vegetable oil Recalled by...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Genova branded Yellowfin Tuna Recalled by Chicken of the Sea; Thai Union Due...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Trader Joe's branded Solid White Albacore Tuna in olive oil Recalled by...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2025· St. Jude Medical

Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...

The Issue: Due to issues associated with data migration of patient information and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2025· Instrumentation Laboratory

Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...

The Issue: Multiple complaints indicating lower than expected quality control (QC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: Optima MR360 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR380 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm and MMT-715 Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing