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 22041–22060 of 29,286 recalls
Recalled Item: FMS neXtra¿ 3.5mm Aggressive Cutter Shaver Blades Recalled by DePuy Mitek,...
The Issue: Product is incorrectly labeled. The blade configuration in the affected lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical Recalled by...
The Issue: Manufacturing error within the Torque Handle may prohibit some handles from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...
The Issue: The firm discovered that information printed on the quick magnet is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number:...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMS 3.5mm Ultra-Aggressive Cutter Shaver Blades Recalled by DePuy Mitek,...
The Issue: Product is incorrectly labeled. The blade configuration in the affected lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization...
The Issue: These screws have a single lead (instead of a triple lead) thread. The screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 Recalled by Boston...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve Recalled by Boston Scientific Corp...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS Recalled by...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests US. Recalled by Biomerieux...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ Recalled by...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...
The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...
The Issue: The treatment table positioning belt can slip gear positions, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...
The Issue: Potential post-processing software issue when using tabcard "4D" on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.