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. 1,983 recalls have been distributed to Virginia in the last 12 months.
Showing 16381–16400 of 29,425 recalls
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Arterial Cannula 22 Fr (O.D.) Recalled by Maquet Cardiopulmonary Ag...
The Issue: This lot of arterial cannula may have been supplied with 3/8-width de-airing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Arterial Cannula 20 Fr (O.D.) Recalled by Maquet Cardiopulmonary Ag...
The Issue: This lot of arterial cannula may have been supplied with 3/8-width de-airing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Arterial Cannula 24 Fr (O.D.) Recalled by Maquet Cardiopulmonary Ag...
The Issue: This lot of arterial cannula may have been supplied with 3/8-width de-airing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...
The Issue: Hyalomatrix products are susceptible to degradation as a result of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microtargeting" Depth Stop Adapter Recalled by FHC, Inc. Due to The FHC...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Motorized) Distributed by Medtronic...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Lead Adapter for microTargeting" Drive Recalled by FHC, Inc....
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.