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 23261–23280 of 29,286 recalls
Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 107" (272 cm) Ext Set w/2 Check Valves Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 113" (287cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 104" (264 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 127" (323cm) Transfer Set w/Check Valve Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 108" (274 cm) Transfer Set w/Check Valve Recalled by ICU Medical, Inc. Due...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 119" (302 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini-Kits Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Kit Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmentation Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Surgical Kits Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.