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. 1,108 recalls have been distributed to Michigan in the last 12 months.
Showing 8021–8040 of 53,342 recalls
Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical TREAT Antifungal Powder Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: CGMP deviations: the product was shipped from the Manufacturer to a Medline...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (SR) Recalled by SUN...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Labeling: Not Elsewhere Classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin synthetic Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Labeling: Not Elsewhere Classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Labeling: Not Elsewhere Classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use...
The Issue: Subpotent: Failing Test Results for Epinephrine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...
The Issue: There is a potential for unexpected failure of the electrical components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...
The Issue: Deterioration in the stability of the Test Strips results in diminished...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI Recalled by...
The Issue: Incorrect pouch labels, the contents within the mislabeled pouch were Roller...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...
The Issue: Sterilization failures when devices are sterilized per the Reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...
The Issue: Unexpected failure of electrical components within the CPI generator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...
The Issue: Due to product outer packaging incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCL 2% and Oxymetazoline HCl 0.025% Solution for intranasal...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Gluconate 2.5% solution for inhalation Recalled by Pine...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropi-Phen (tropicamide 1% Recalled by Pine Pharmaceuticals, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection Recalled by Pine...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.