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. 1,077 recalls have been distributed to Michigan in the last 12 months.
Showing 15541–15560 of 53,342 recalls
Recalled Item: uMI 550 System - Product Usage: intended to be operated Recalled by Shanghai...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow sensors that may be installed in the following GEHC Recalled by GE...
The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steripath Luer Transport Pack Recalled by Magnolia Medical Technologies,...
The Issue: Product was shipped with the incorrect Transfer Adapter Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clopidogrel Tablets Recalled by Macleods Pharma Usa Inc Due to Presence of...
The Issue: Presence of foreign matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 365 SKINNY High Intensity Capsules Recalled by Je Dois Lavoir LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artificial Tears Ointment Recalled by Akorn, Inc. Due to Non-Sterility - OOS...
The Issue: Non-Sterility - OOS sterility testing observed during 12-month controlled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FLUDARABINE PHOSPHATE FOR INJECTION Recalled by Custopharm, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: the manufacturing firm had microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...
The Issue: Sling loop straps on device pose a trip hazard.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...
The Issue: Product may not perform as specified in IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...
The Issue: A thin wall condition between the inner cannulation and the flutes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.