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. 1,009 recalls have been distributed to Virginia in the last 12 months.
Showing 33661–33680 of 53,829 recalls
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Phosphate and Benzoyl Peroxide Gel Recalled by L. Perrigo...
The Issue: Microbial Contamination of Non-Sterile Product; small number of tubes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Recalled by The Two...
The Issue: Joe Chips Sour Cream & Toasted Onion Retro Potato Chips contains a seasoning...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES Recalled by Roland Foods,...
The Issue: Product quality issue. Through sampling, FDA revealed the presence of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...
The Issue: May experience a loss of centralized monitoring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC 9800...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9900 Elite. MDL Numbers: D148942 Recalled by GE OEC Medical Systems, Inc...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC 9800...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...
The Issue: The affected products have approximately a 91% specificity while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.