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. 2,698 recalls have been distributed to Michigan in the last 12 months.
Showing 7461–7480 of 53,342 recalls
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waiakea Hawaiian Volcanic Water Naturally Alkaline Electrolytes Deep Well...
The Issue: Consumer complaints involving floating particles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Mobile...
The Issue: Mobile x-ray system can report and deliver a lower post-exposure mAs value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortera Spinal Fixation System Recalled by XTANT Medical Holdings, Inc Due...
The Issue: Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Packaged Recalled by AtriCure, Inc. Due to AtriCure has identified certain...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryo Module Accessories Domestic CMA-OUS Recalled by AtriCure, Inc. Due to...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volar Bearing Plate. Recalled by TriMed Inc. Due to Plates, part of a wrist...
The Issue: Plates, part of a wrist fixation system, are affixed during surgery with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Patient Information Center iX Recalled by Philips North America Due to...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CareEvent Recalled by Philips North America Due to Push notifications...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER pedicle system Recalled by Icotec Ag Due to icotec has received...
The Issue: icotec has received notification of one revision that had to be carried out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYNXGRIP 5F Recalled by Cordis US Corp Due to Cordis became aware that the...
The Issue: Cordis became aware that the label for the carton box containing 10 units is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER pedicle system Recalled by Icotec Ag Due to icotec has received...
The Issue: icotec has received notification of one revision that had to be carried out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYNXGRIP 6F/7F Recalled by Cordis US Corp Due to Cordis became aware that...
The Issue: Cordis became aware that the label for the carton box containing 10 units is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS 3 CSF External Drainage System Recalled by Natus Medical Incorporated...
The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.