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. 2,722 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,722 in last 12 months

Showing 52415260 of 13,418 recalls

DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Cisplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey Inc....

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Fentanyl Citrate Active Pharmaceutical Ingredient Recalled by Johnson...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Oxaliplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2019· AVKARE Inc.

Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...

The Issue: Failed Stability Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2019· American Health Packaging

Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...

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

Class III — Low RiskOngoing
Refund
DrugAugust 24, 2019· Tuscano and Delucia Group (DBA Entropic Labs)

Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...

The Issue: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: fexofenadine hydrochloride tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine HCL Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochrloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine HCl) tablets USP Recalled by Aurolife Pharma,...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (fexofenadine hydrochrloride) tablets Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2019· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...

The Issue: Subpotent Drug: Out of specification result during stability study in...

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

Class III — Low RiskOngoing
Refund
DrugAugust 16, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2019· Pfizer Inc.

Recalled Item: RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: contamination with...

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

Class II — Potential Health HazardOngoing
Refund