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 24081–24100 of 53,342 recalls
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...
The Issue: Small black plastic particle was observed in the left ventricle during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Sponge with the following product description and model numbers:...
The Issue: Potential lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Small Diameter Cement Plug Inserter-Sterile Recalled by Zimmer...
The Issue: Lack of an adequate sterilization validation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnidiagnost Classic Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Syringe Administration Set-Product Package Size 50 Recalled by...
The Issue: Leaking of the Smartsite Syringe Administration Set. May result in delay or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.