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. 2,564 recalls have been distributed to Michigan in the last 12 months.
Showing 17901–17920 of 29,286 recalls
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled...
The Issue: Three (3) complaints were identified in which the potential for utilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaSafe Plastic Cannula - 11 Gauge Recalled by CareFusion 303, Inc. Due to...
The Issue: Punctures in blister packaging that was detected during the packaging process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...
The Issue: The table shift in the vertical direction was inverted during the use of CMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...
The Issue: Replacement campaign on all units that have a gas spring head in aluminum.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PPS RingLoc+ Acetabular Shell Recalled by Zimmer Biomet, Inc. Due to Device...
The Issue: Device was distributed with the etching missing from the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.