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. 2,807 recalls have been distributed to Virginia in the last 12 months.
Showing 8301–8320 of 53,829 recalls
Recalled Item: BREG WALKER FOLDING WALKER WITH WHEELS Utilized as Recalled by Breg Inc Due...
The Issue: Due to walkers not meeting product specifications. Walkers were manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 and Astral 150 ventilators Recalled by ResMed Ltd. Due to If...
The Issue: If ventilator is on internal battery, not intended to serve as a primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The firm has investigated and confirmed that when DxI 9000 is connected to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Plus Aerobic/F Culture Vials Recalled by Becton Dickinson & Co....
The Issue: Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eligard (leuprolide acetate) for injectable suspension Recalled by Tolmar,...
The Issue: Superpotent Drug - Higher than expected levels of leuprolide acetate in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LittleOak Natural Goat Milk Infant Formula (Stage 1) Recalled by The Little...
The Issue: No pre-market notification and Mixing instructions not in ounces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LittleOak Natural Goat Milk Follow On Infant Formula (Stage 2) Recalled by...
The Issue: No pre-market notification and Mixing instructions not in ounces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.