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. 2,537 recalls have been distributed to Michigan in the last 12 months.
Showing 21321–21340 of 29,286 recalls
Recalled Item: 1) VITROS¿ Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique...
The Issue: When testing was conducted using certain lots, VITROS¿ Systems generated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acorn 180 Curved Stairlift Recalled by Acorn Stairlifts Inc Due to Aluminum...
The Issue: Aluminum rivets holding the base squab to the framer under prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ adjust aluminum crutch under the following labels: 1) EZ Recalled by...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aluminum crutch under the following labels: 1) Aluminum crutch Recalled by...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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 safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal aluminum crutch Recalled by Medical Depot Inc. Due to Tip crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Direct Supply aluminum crutch Recalled by Medical Depot Inc. Due to Tip...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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 safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Applied...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilson Implantation System Product Usage: Indicated to aid in tissue...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.