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. 1,077 recalls have been distributed to Michigan in the last 12 months.
Showing 15661–15680 of 53,342 recalls
Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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: 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: 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: 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 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 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 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 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: 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 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: 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: EPIQ Ultrasound Systems Recalled by Philips Ultrasound Inc Due to Ultrasound...
The Issue: Ultrasound system control panel arm swivel lock could fail, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.