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. 2,670 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,670 in last 12 months

Showing 77817800 of 52,000 recalls

FoodOctober 23, 2023· Gills Onions, LLC

Recalled Item: Cross Valley Farms 2/5 LB CTN FRESH 1/2" DICED YELLOW ONIONS W/ZIP Recalled...

The Issue: Potential contamination with Salmonella Thompson

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 23, 2023· Gills Onions, LLC

Recalled Item: 4/5 LB CTN FRESH 1/4" DICED YLW ONIONS W/ZIPPER DARDEN Recalled by Gills...

The Issue: Potential contamination with Salmonella Thompson

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 23, 2023· Gills Onions, LLC

Recalled Item: PEAK 4/5 LB CTN FRESH 1/4" DICED YELLOW ONIONS W/ZIPPER Recalled by Gills...

The Issue: Potential contamination with Salmonella Thompson

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 23, 2023· Gills Onions, LLC

Recalled Item: PEAK 2/5 LB CTN FRESH 1/2" DICED YELLOW ONIONS W/ZIP Recalled by Gills...

The Issue: Potential contamination with Salmonella Thompson

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 23, 2023· Gills Onions, LLC

Recalled Item: Gills Onions 2/5 LB CTN FRESH 3/8" DICED RED ONIONS WITH ZIPPER Recalled by...

The Issue: Potential contamination with Salmonella Thompson

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

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

Class II — Potential Health HazardOngoing
DrugOctober 20, 2023· Botanical Be

Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· ITF PHARMA INC

Recalled Item: Tiglutik (riluzole) Oral Suspension 50 mg/10 mL (5 mg/mL) Recalled by ITF...

The Issue: Failed Viscosity Specifications: Out-of-specification test results for viscosity

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· Zyla Life Sciences US Inc.

Recalled Item: Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to...

The Issue: Sub-potent Drug: Lower potency than labeled.

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Failed Impurities/Degradation Specifications.

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

Class II — Potential Health HazardOngoing
Refund