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. 2,722 recalls have been distributed to Michigan in the last 12 months.
Showing 4741–4760 of 53,342 recalls
Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems Recalled by Siemens...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper 1.0 Recalled by Siemens Medical Solutions USA, Inc. Due to If...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE LONG VERSION Recalled by B Braun Medical Inc Due to...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module Model 8120 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE LONG-Tubing to be used to transfer blood between a Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.