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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1916119180 of 53,342 recalls

DrugMay 26, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Olanzapine Tablets Recalled by Aurobindo Pharma USA Inc. 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 26, 2020· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...

The Issue: Failed Impurities/Degradation Specifications: potential migration of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· The Harvard Drug Group

Recalled Item: Doxycycline Hyclate Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specification: The dissolution test at the 24 month time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2020· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F Recalled...

The Issue: Due to adverse events received by the firm for left atrial perforations and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...

The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...

The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2020· Vitalconnect Inc.

Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...

The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System - Software Versions 3.3.3 and Recalled by...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software Versions 3.3.3 and below Product...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System - Product Code: 6802914 Unique Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing