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. 1,139 recalls have been distributed to Michigan in the last 12 months.
Showing 1321–1340 of 53,342 recalls
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...
The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.