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. 2,747 recalls have been distributed to Michigan in the last 12 months.
Showing 301–320 of 29,286 recalls
Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Precision IV Pump Recalled by ICU Medical, Inc. Due to...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Infusion Pump Recalled by ICU Medical, Inc. Due to Plum...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is...
The Issue: Potential for defect for Asserachrom HPIA lot 271288, which can affect every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Solo Precision IV Pump Recalled by ICU Medical, Inc. Due to...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Recalled by Intuitive Surgical, Inc. Due to Access Port System...
The Issue: Access Port System tray may develop cracks potentially resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER...
The Issue: Product contains potentially harmful dosing errors for Vecuronium,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10F Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Recalled by Immunotech A.S. Due to The affected Estrone RIA kit...
The Issue: The affected Estrone RIA kit lots may rarely give falsely high patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number:...
The Issue: The console label for affected devices is missing the "DANGER" symbol.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...
The Issue: Under specific conditions, the lift's electromagnetic holding force may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.