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. 2,747 recalls have been distributed to Michigan in the last 12 months.
Showing 281–300 of 53,342 recalls
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use Sphincterotome V (Distal Wire guided) Model/Catalog...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HerbsForever- Hingwastika Churna Recalled by Herbs Forever Due to Undeclared...
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AQ 120 GFEW Recalled by Encon Safety Products Co Due to cGMP deviations.
The Issue: cGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...
The Issue: The mix up of the impression caps provided in the package. The provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.