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. 2,652 recalls have been distributed to Michigan in the last 12 months.
Showing 15661–15680 of 53,342 recalls
Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...
The Issue: Due to potential performance issues with software version 3.2.3 and earlier....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick Recalled by...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Prep Pad Large Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Swabstick (3's) Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Prep Pad MEDIUM Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodide Cleansing Scrub Swabstick (3's) Recalled by Professional...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidine Iodine Swabstick (1's) Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...
The Issue: The kit contains the wrong vial tray in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter prismaflex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PrismaFlex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.