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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 2201–2220 of 53,342 recalls
Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...
The Issue: Due to an incorrect test results provided that indicated the incorrect drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-view video laryngoscope. Model Number: 8008000. The i-view video...
The Issue: Potential for faulty devices as a result of depleted batteries.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2645 - Nonpareils Recalled by Weaver Nut Company, Inc Due to Undeclared Milk
The Issue: undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 47518 - Nonpareil Recalled by Weaver Nut Company, Inc Due to Undeclared Milk
The Issue: undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weaver Chocolates Recalled by Weaver Nut Company, Inc Due to Undeclared Milk
The Issue: Undeclared Milk Allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weaver Chocolates Recalled by Weaver Nut Company, Inc Due to Undeclared Milk
The Issue: Undeclared Milk Allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Lack of assurance of sterility: pinholes, within the finger boxes used...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...
The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...
The Issue: Closed system drug transfer devices were shipped to the U.S. market without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...
The Issue: Reports of IVUS catheter and guide wire entanglement during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...
The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.