Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,436 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,436 in last 12 months

Showing 3944139460 of 52,000 recalls

Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...

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· GE Healthcare

Recalled Item: GE Healthcare Innova 2100IQ. 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· AGFA Healthcare Corp.

Recalled Item: AGFA DX-D 100 is a mobile digital radiography x-ray system Recalled by AGFA...

The Issue: When using the DX-D 100 unit, sporadic unintended movements caused by an...

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

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

Recalled Item: Sureflex 150 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
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: 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: 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: 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: 200¿M Lithotripsy Fiber- Reusable 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
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 365 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
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: 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