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. 2,563 recalls have been distributed to Michigan in the last 12 months.
Showing 18841–18860 of 29,286 recalls
Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...
The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The JETSTREAM is a rotational atherectomy catheter system designed for...
The Issue: Boston Scientific is initiating a voluntary removal of two lots of JETSTREAM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...
The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun 5000 Temperature Management System Recalled by C.R. Bard, Inc....
The Issue: Potential failure of the Arctic Sun 5000 Temperature Management System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...
The Issue: Medtronic is issuing a voluntary field corrective action for all its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.