Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,666 in last 12 months

Showing 58215840 of 13,424 recalls

DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: B-complex (Thiamine 100mg Recalled by Pharm D Solutions, LLC Due to Lack of...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: Nandrolone Decanoate 200 mg/mL Injectable Recalled by Pharm D Solutions, LLC...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 & 6 (3-3-3 MG) vials Recalled by Pharm D Solutions, LLC...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Complaint received of metal piece identified in the product bottle prior to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2019· Fresenius Kabi USA, LLC

Recalled Item: Ondansetron Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2019· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2019· MALLINCKRODT PHARMACEUTICALS

Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...

The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· MALLINCKRODT PHARMACEUTICALS

Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...

The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2019· Novartis Pharmaceuticals Corp.

Recalled Item: Promacta (eltrombopag) 12.5 mg for Oral Suspension Recalled by Novartis...

The Issue: Cross Contamination with Other Products: product is being recalled due to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2019· Ecolab Inc

Recalled Item: QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol) Recalled by...

The Issue: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong...

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

Class III — Low RiskOngoing
Refund
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2019· American Health Packaging

Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...

The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Zydus...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 6, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.25 mg Recalled by Zydus...

The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...

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

Class II — Potential Health HazardOngoing
Refund