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. 1,936 recalls have been distributed to Virginia in the last 12 months.
Showing 21681–21700 of 29,425 recalls
Recalled Item: Product 2 consists of all products product code LPH Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 6 consists of all products under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 55 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...
The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 58 consists of all product under product code: HRS Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 38 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 33 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 11 consists of all product under product code JDI Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 57 consists of all product code: JDI and same Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 39 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 50 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 9 consists of all product under HRS Recalled by Zimmer Manufacturing...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 32 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Microsystems (Schweiz) Ag. The common name of the device Recalled by...
The Issue: An electronic component of the Leica M525 OH4 and Leica M720 OH5 surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 41 consists of all product under product code: KTT Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 VERSYS 6 INCH BEADED Recalled by Zimmer Biomet,...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 26 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 49 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 47 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Knee CR Porous FEM NexGen Knee CR Precoat FEM prosthesis Recalled by...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.