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. 2,673 recalls have been distributed to Michigan in the last 12 months.
Showing 13581–13600 of 53,342 recalls
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Product: Product is contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Acetate Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...
The Issue: Presence of particulate matter: particulates composed of carbon and oxygen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per...
The Issue: Dietary supplement may contain potential metal shavings greater than or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...
The Issue: The product was distributed without FDA authorization or clearance for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....
The Issue: Software issue resulting in temporary loss of central monitoring functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...
The Issue: During the de-installation of an MR system magnet, if all rigging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m HBV AMP Kit (US and CE) Recalled by Abbott Molecular, Inc. Due to...
The Issue: There is a potential for misquantitation high results for negative samples.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...
The Issue: Sterility failure of the exterior of the syringe which may impact the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m HBV Application Specification File (US and CE) Recalled by Abbott...
The Issue: There is a potential for misquantitation high results of negative samples.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VESSEL SEALER EXTEND Recalled by Intuitive Surgical, Inc. Due to Placing...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi' Recalled by Intuitive...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 1) UPN:M0054242CE0 Intended Use:...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.