Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,541 in last 12 months

Showing 34013420 of 13,356 recalls

DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: MidNite Natural sleep aid Chewable Tablets Cherry Flavor (melatonin 1.5mg)...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PEPTIME Energy (caffeine 300mg) tablets Recalled by Ultra Seal Corporation...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Ephedrine Plus (Ephedrine HCl 25mg Recalled by Ultra Seal Corporation Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: DILOTAB II Recalled by Ultra Seal Corporation Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg Recalled by Ultra...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Cold/Sinus Pain Reliever/Fever Reducer Nasal Decongestant (acetaminophen 325...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PAINAID PMF Premenstrual Formula (acetaminophen 500 mg Recalled by Ultra...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: MidNite Sleep Health (melatonin 1.5 mg) tablets Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Nutralox Mint Antacid (calcium carbonate 420mg) Chewable tablets Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PAINAID (acetaminophen 110 mg Recalled by Ultra Seal Corporation Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Cold Relief (acetaminophen 250 mg Recalled by Ultra Seal Corporation Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: CONGESTAID II Nasal Decongestant (Phenylephrine HCl 5mg) 2 tablet packets...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%)...

The Issue: cGMP deficiencies

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2022· Teva Pharmaceuticals USA

Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...

The Issue: Failed Dissolution Specification: Dissolution results are below...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2022· Mayne Pharma Inc

Recalled Item: Lexette (halobetasol propionate) Topical Foam Recalled by Mayne Pharma Inc...

The Issue: CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid...

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

Class II — Potential Health HazardOngoing
Refund