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 721–740 of 29,286 recalls
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed...
The Issue: Due to an issue (potential breakage) with the shaft for the mounting of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER BICARBONATE OSR6237 OSR6637 OSR6x37 Bicarbonate is Recalled...
The Issue: Bicarbonate reagent may generate falsely high Bicarbonate results due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V...
The Issue: Continued reports of positive cultures and infections have identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Luer Tip Caps Recalled by Becton Dickinson & Company Due to BD has...
The Issue: BD has confirmed through internal testing that certain device trays failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI LED Mobile Exam Light Battery This non-magnetic Recalled by MRIMed Inc....
The Issue: Due to battery component overheating while charging resulting in melting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom Fibula Nail Recalled by Paragon 28, Inc. Due to Fibula nail system...
The Issue: Fibula nail system intended for use in fixation of fibular fractures and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Blood Pump Recalled by Thoratec LLC Due to Acute circulatory...
The Issue: Acute circulatory support system pump may not fit into the motor and reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kit Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.