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. 2,520 recalls have been distributed to Michigan in the last 12 months.
Showing 28081–28100 of 29,286 recalls
Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System Inserter Stainless Steel Recalled by Zimmer,...
The Issue: Zimmer Spine is has received complaints of difficulty in turning the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...
The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...
The Issue: The Back Table Cover component in the custom pack was placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...
The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Flow Module indicated for use Recalled by...
The Issue: Terumo Cardiovascular Systems (CVS) received one report of a flow module for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware that patient mismatch without a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.