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 3101–3120 of 29,286 recalls
Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S -For use as a diagnostic device to Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...
The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar Injector And Syringe Recalled by Merit...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...
The Issue: It has been determined that certain Blood Pressure Monitors containing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device MAP 112 Access-9 Large Bore Hemostasis Value...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...
The Issue: It has been determined that certain Blood Pressure Monitors containing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...
The Issue: It has been determined that certain Blood Pressure Monitors containing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trevo Trak 21 Microcatheter is a single-lumen Recalled by Stryker...
The Issue: Stryker Neurovascular has observed that devices with Out of United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Tee T-Piece Resuscitator. Part Numbers 1050805 Recalled by Mercury...
The Issue: Manual resuscitator circuit flow controller may come apart due to a missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to The...
The Issue: The software has anomalies that have the potential to cause alarms,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 (Model Number 866060) Recalled by Philips...
The Issue: During a production process, Philips became aware of one IntelliVue power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.