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. 2,848 recalls have been distributed to Virginia in the last 12 months.
Showing 1501–1520 of 53,829 recalls
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Product Codes: (1)722013 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Product Codes: (1)722011 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table Product Codes: (1)722022 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Product Codes: (1)722010 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 OR Table Product Codes: (1)722023 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Product Codes: (1)722020 Recalled by...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Product Codes: (1)722012 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norgestimate and Ethinyl Estradiol Tablets Recalled by AvKARE Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tribio Implant 7.5mm x 40mm SB008 UDI code: Recalled by Berkeley Advanced...
The Issue: Due to incorrect product label (Incorrect product name identified on outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...
The Issue: The bovine carotid arteries used to produce the impacted grafts from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.