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. 2,507 recalls have been distributed to Michigan in the last 12 months.
Showing 35981–36000 of 53,342 recalls
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID Recalled by CMP Industries, Llc...
The Issue: Possible presence of foreign material (rust).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Recalled by...
The Issue: Due to the buildup of grease within the hose and motor, the product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...
The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAK Liquid Acrylic Resin sold under the following labels: 1) Recalled by...
The Issue: Possible presence of foreign material (rust).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.