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 23821–23840 of 29,286 recalls
Recalled Item: ABL90 FLEX analyzer Recalled by Radiometer America Inc Due to The ABL90...
The Issue: The ABL90 analyzer does not always use the most recent calibration data to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...
The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osteobond Bone Cement Bone cement monomer is kitted with bone Recalled by...
The Issue: Samples of product from Supplier lot 14D0809 and 14D0808 showed little...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...
The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verasense Knee System Recalled by Orthosensor, Inc. Due to Presence of one...
The Issue: Presence of one inoperable (dead) sensor pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...
The Issue: Invacare identified that the rail mounting bracket on the G29 full length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial Broach Inserter/Extractor. The Persona Cemented...
The Issue: The affected lot was supplied by contract manufacturer and are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Servo Humidifier 163 Recalled by Teleflex, Inc. Due to Connector...
The Issue: Connector mount cracks which may lead to a leak failure during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUX Material Recalled by Trumpf Medical Systems, Inc....
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...
The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.