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. 1,780 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,780 in last 12 months

Showing 4098141000 of 53,829 recalls

Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The PowerLED / X-TEN / VOLISTA Surgical Light Systems are Recalled by Maquet...

The Issue: Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2015· Apotex Inc.

Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...

The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMay 29, 2015· Walgreen Company

Recalled Item: Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a Recalled by Walgreen...

The Issue: Nice! Powdered Sugar Mini Donuts may contain mold. Alleged illnesses have...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2015· Byrd Cookie Co

Recalled Item: Byrds Famous Cookies Recalled by Byrd Cookie Co Due to Undeclared Anchovies

The Issue: Undeclared Anchovies

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2015· Byrd Cookie Co

Recalled Item: Byrds Famous Cookies Recalled by Byrd Cookie Co Due to Undeclared Anchovies

The Issue: Undeclared Anchovies

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Synthes, Inc.

Recalled Item: Pull Reduction Device For 4.3mm Percutaneous Drill Guide Recalled by...

The Issue: Certain affected parts and lots of the Pull Reduction Devices may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 910 Lithotripsy Fiber Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing