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. 2,498 recalls have been distributed to Michigan in the last 12 months.
Showing 38201–38220 of 53,342 recalls
Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube Recalled by Geritrex Corp Due...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets USP Recalled by Par Pharmaceutical Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: David Trail Mix Sweet & Salty individual plastic bags net Recalled by...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mountain Mix 2oz bag Recalled by Kanan Enterprises, Inc. Due to Undeclared Milk
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kings fresh & Delicious Cashews & Sweeties Net Wt. 14oz. Recalled by Kanan...
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sweet & Salty Mix 2.75oz Tube Bag Recalled by Kanan Enterprises, Inc. Due to...
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential issue with routine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon Dry Acid Dissolution Unit Recalled by Fresenius Medical...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...
The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iOS Galileo Application Version 1.1.1 or lower that programs the Recalled by...
The Issue: A software issue can make the foot move into dorsiflexion, unnoticed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.