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. 2,849 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,849 in last 12 months

Showing 10811100 of 53,829 recalls

Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2025· Mohamed Hagar

Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 8, 2025· Tai Foong USA Inc

Recalled Item: Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 Recalled...

The Issue: Undeclared shrimp

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 8, 2025· Sprouts Farmers Market

Recalled Item: Sprouts Smoked Mozzarella Pasta Salad Recalled by Sprouts Farmers Market Due...

The Issue: Product may contain Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 8, 2025· ASTRAZENECA PHARMACEUTICALS

Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...

The Issue: Lack of Assurance of Sterility:

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2025· Cellavision AB

Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...

The Issue: Automated cell-locating device barcode reader may read the barcode of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...

The Issue: The device may either fail to start up, or the transducer may start briefly...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Rising Pharma Holding, Inc.

Recalled Item: Carbidopa Recalled by Rising Pharma Holding, Inc. Due to Product mix up:...

The Issue: Product mix up: complaint received that sealed medication bottle contained...

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

Class II — Potential Health HazardOngoing
Refund