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. 1,121 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,121 in last 12 months

Showing 2861–2880 of 52,000 recalls

DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ranolazine Extended-Release Tablets 1000mg Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Cetirizine Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Levetiracetam 0.75% in Sodium Chloride Injection 1 Recalled by Dr. Reddy's...

The Issue: LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 13, 2025· Seabear Company

Recalled Item: SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch...

The Issue: Recall was initiated due to potential failure of the seal and potential to...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2025· Seabear Company

Recalled Item: SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch...

The Issue: Recall was initiated due to potential failure of the seal and potential to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Recalled by...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
DrugMarch 12, 2025· Alchemee, LLC

Recalled Item: Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) Recalled by...

The Issue: Chemical contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
DrugMarch 12, 2025· Alchemee, LLC

Recalled Item: Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) Recalled by...

The Issue: Chemical contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
FoodMarch 12, 2025· FRUSELVA USA

Recalled Item: Good & Gather baby Pea Recalled by FRUSELVA USA Due to elevated level of lead

The Issue: elevated level of lead

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number:...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
DrugMarch 11, 2025· Fruit Of The Earth, Inc.

Recalled Item: Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl...

The Issue: Chemical contamination: presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2025· FDC Limited

Recalled Item: Ciprofloxacin Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: Unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2025· Bard Access Systems, Inc.

Recalled Item: BD 4 Fr Single-Lumen PowerPICC Catheters Recalled by Bard Access Systems,...

The Issue: Catheters indicated for short-or-long term access to the central venous...

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

Class I — Serious Health HazardOngoing
DrugMarch 11, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2025· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...

The Issue: Users trying to restock a single bin location of an automated dispensing...

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

Class II — Potential Health HazardOngoing