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 26212640 of 53,829 recalls

Medical DeviceMay 6, 2025· Baxter Healthcare Corporation

Recalled Item: Affinity 4 Birthing Bed Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for improper crimps on the signal wires of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Copan WASP

Recalled Item: PhenoMATRIX Recalled by Copan WASP Due to AI-powered bacterial culture plate...

The Issue: AI-powered bacterial culture plate interpretation and workup software does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V Recalled...

The Issue: Recent post-market surveillance data suggests a possible association of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2025· Dexcom, Inc.

Recalled Item: Dexcom G7 iOS Application Recalled by Dexcom, Inc. Due to A bug in the 2.7.0...

The Issue: A bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a...

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

Class II — Potential Health HazardOngoing
FoodMay 2, 2025· East CK Trading Inc.

Recalled Item: President Brand Licorice Plum (8 oz. Recalled by East CK Trading Inc. Due to...

The Issue: Contains undeclared sulfites, undeclared FD&C Yellow 6, and unapproved...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2025· Vietti Acquisitions, LLC

Recalled Item: Yellowstone Brown Sugar Molasses Baked Beans Recalled by Vietti...

The Issue: Undeclared allergen (soy) due to mislabeling. Product is labeled as Brown...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 2, 2025· Empower Clinic Services, LLC dba Empower Pharmacy

Recalled Item: Testosterone Cypionate Injection Recalled by Empower Clinic Services, LLC...

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 DeviceMay 2, 2025· Copan Italia

Recalled Item: BD BBL CultureSwab EZ Collection and Transport System Recalled by Copan...

The Issue: Swabs for specimen collection may be prone to breakage during product usage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Healthmark Industries Co., Inc.

Recalled Item: ChannelCheck Convenience Pack Recalled by Healthmark Industries Co., Inc....

The Issue: During endoscope surveillance monitoring, a user facility identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160341 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Healthmark Industries Co., Inc.

Recalled Item: Pre-filled Water Syringe Recalled by Healthmark Industries Co., Inc. Due to...

The Issue: During endoscope surveillance monitoring, a user facility identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160119 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160325 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160333 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160648 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· Cardinal Health 200, LLC

Recalled Item: Catalog No. 8888160556 Recalled by Cardinal Health 200, LLC Due to Packaging...

The Issue: Packaging defect may compromise sterility of the product. Use of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2025· ICU Medical, Inc.

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

The Issue: Firm has identified Drug Library Management defects in the software: 1) DLM...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2025· Implant Direct Sybron Manufacturing LLC

Recalled Item: The Drill Stop Kit is the version of the Mini Recalled by Implant Direct...

The Issue: The Drill stop kit contains incorrect components.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2025· Remel, Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth...

The Issue: Product may have an off color affecting perfomance

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

Class II — Potential Health HazardOngoing