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 12811300 of 53,829 recalls

DrugSeptember 19, 2025· Ascend Laboratories, LLC

Recalled Item: Atorvastatin Calcium Tablets USP Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2025· Ascend Laboratories, LLC

Recalled Item: Atorvastatin Calcium Tablets USP Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2025· Ascend Laboratories, LLC

Recalled Item: Atorvastatin Calcium Tablets USP Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2025· Ascend Laboratories, LLC

Recalled Item: Atorvastatin Calcium Tablets USP Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2025· Orthofix U.S. LLC

Recalled Item: Virata Preassembled Polyaxial Screw Recalled by Orthofix U.S. LLC Due to...

The Issue: Polyaxial screws do not meet performance standards.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2025· Beckman Coulter, Inc.

Recalled Item: DxC 500i Clinical Analyzer Modules Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2025· Kico Knee Innovation Company

Recalled Item: Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number:...

The Issue: Complaint identified issue with AI surgical planning software that may...

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

Class II — Potential Health HazardOngoing
FoodSeptember 18, 2025· Goyal Group Inc.

Recalled Item: 1. SILVER HORSE - PURE ALUMINIUM MADE IN INDIA - Recalled by Goyal Group...

The Issue: Contains elevated levels of lead

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Western United Fish Company Inc

Recalled Item: Kirkland Signature brand Ahi Tuna Wasabi Poke Recalled by Western United...

The Issue: Listeria monocytogenes. Recall was initiated after being notified by green...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Recalled...

The Issue: Software issue for hq analyzer results in system not visibly applying...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump"...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· HeartSine Technologies Ltd

Recalled Item: HeartSine Pad-Pak Recalled by HeartSine Technologies Ltd Due to Due to...

The Issue: Due to customer complaints, defibrillator pads may contain damage pins that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· GE Medical Systems, LLC

Recalled Item: LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7....

The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· GE Medical Systems, LLC

Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....

The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...

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

Class II — Potential Health HazardOngoing