Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,552 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,552 in last 12 months

Showing 34013420 of 13,407 recalls

DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Extra Strength (ES) PAIN RELIEVER (acetaminophen 500 mg) 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 24, 2022· Ultra Seal Corporation

Recalled Item: PEPTIME Energy (caffeine 250mg) 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: EXTRA STRENGTH UN-ASPIRIN (acetaminophen 500 mg) 2 Caplet packets Recalled...

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: Exaprin pain reliever (acetaminophen 110 mg 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: SINU-PHEN PLUS sinus pain and congestion tabs (acetaminophen 500 mg Recalled...

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 Severe Pain/Cough (acetaminophen 325mg 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: AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) 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: Regular Strength Pain Reliever (acetaminophen 110 mg 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: Cold Tablet Pain Reliever/Fever Reducer/Expectorant/Nasal Decongestant...

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: SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets...

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: REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 mg) Caplets 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: CETAFEN COUGH & COLD COUGH & 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: ELECTROLYTE Supplement Tablets (calcium 5.2 mg 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: Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg) Recalled...

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: 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 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