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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1086110880 of 52,000 recalls

Medical DeviceDecember 5, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...

The Issue: Pod may have weld failures breaching the sterile barrier and result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...

The Issue: Pod may have weld failures breaching the sterile barrier and result in the...

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

Class II — Potential Health HazardOngoing
FoodDecember 5, 2022· Cranberry Sweets & More Inc

Recalled Item: Recalled Meltaways product is packaged in clear cellophane bags Recalled by...

The Issue: Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 5, 2022· Northern Food I/E Inc.

Recalled Item: Beijing Hawthorne Candy Recalled by Northern Food I/E Inc. Due to Undeclared...

The Issue: Product contains undeclared sulfites (7.32 mg/serving)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Integra LifeSciences Corp.

Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...

The Issue: Integra LifeSciences identified that one lot was released with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro Monofilament Polypropylene Sutures Product Description CP-535...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Tomy International Inc.

Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...

The Issue: Affected lots of the product are being recalled due to potential microbial...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro II Monofilament Polypropylene Sutures Product Description Model...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund