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. 1,122 recalls have been distributed to Virginia in the last 12 months.
Showing 9141–9160 of 29,425 recalls
Recalled Item: REF/Catalogue Number GSXE0030B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030H Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0025A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0030 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0020 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0020A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.