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. 2,710 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,710 in last 12 months

Showing 701720 of 52,000 recalls

Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Inner Sheath Recalled by Olympus Corporation of the...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model Recalled by...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic Recalled by...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC MORINGA LEAF POWDER Recalled by Lexunder Inc Due...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC SUPERGREENS POWDER MIX Recalled by Lexunder Inc...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 11, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Varenicline Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Sub...

The Issue: Sub potent drug: during the 9-month stability test conducted, the assay...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing