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. 2,532 recalls have been distributed to Michigan in the last 12 months.
Showing 28861–28880 of 53,342 recalls
Recalled Item: DARK CHOCOLATE CRANBERRY Recalled by Rocky'S Historic Eastern Market Due to...
The Issue: Rocky s Historic Eastern Market initiated a voluntary recall of DARK...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DARK CHOCOLATE CHERRY Recalled by Rocky'S Historic Eastern Market Due to...
The Issue: Rockys Historic Eastern Market initiated a voluntary recall of DARK...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bean Boy Coffee Dark Chocolate Covered Espresso Beans Recalled by Pacific...
The Issue: Pacific Rim Distribution Inc., dba Bean Boy Coffee is voluntarily recalling...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.