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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 1521–1540 of 29,286 recalls
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i SETpoint Calibrator Recalled by Siemens Healthcare...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROSKOP Omnia. Model Number: 10094910 Recalled by Siemens Medical Solutions...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROSKOP Omnia Max. Model Number: 10762473 Recalled by Siemens Medical...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...
The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...
The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...
The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...
The Issue: Bone external fixation system may have the pin that can become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Recalled...
The Issue: Due to a risk of false positive results that could lead to unnecessary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....
The Issue: Kit USB flash drive contains outdated software, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.