Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,081 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,081 in last 12 months

Showing 13941–13960 of 53,342 recalls

DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Bumetanide Tablets Recalled by CARDINAL HEALTHCARE Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Low Dose ASPIRIN Recalled by CARDINAL HEALTHCARE Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Donepezil HCl Tablets Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: FIRST LANSOPRAZOLE PT 3MG/ML Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 25, 2022· Blaine Labs Inc

Recalled Item: REVITADERM WOUND CARE GEL Recalled by Blaine Labs Inc Due to Microbial...

The Issue: Microbial Contamination of Non-sterile Product; FDA analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: PAINAID BRF Back Relief Formula (acetaminophen 250 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: CVS Health Natural Sleep Aid Chewable Tablets Cherry Flavor (melatonin...

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: Nasal & Sinus Decongestant (phenylephrine HCl 5mg) 2 tablets per packet...

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 Non-aspirin pain reliever (acetaminophen 325mg) 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: 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: 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: PEPTIME Energy (caffeine 350mg) 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: FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 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 Cold Relief (acetaminophen 325 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: PAPENOL (acetaminophen 500 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: Headache & Congestion Sinus Relief (acetaminophen 250 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: PAIN TERMINATOR extra strength pain relief (aspirin 162 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: Pain Away Pain Reliever/Fever Reducer (NSAID) (acetaminophen 110 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: Sinus Relief Headache/Nasal (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: MAGNACAL (calcium carbonate 420 mg) Recalled by Ultra Seal Corporation Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund