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 25641–25660 of 29,286 recalls
Recalled Item: PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY)...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Non-Vented Recalled by Medtronic...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intersept Custom Tubing Pack which contain Select 3D or Recalled...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...
The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168...
The Issue: Customers were unable to calibrate, or use previously calibrated, VITROS DT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the...
The Issue: Unapproved material used by vendor in subset of shorts causing them to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Mandible Short Threaded Drill Guide intended for oral...
The Issue: One lot of Matrix Mandible Short Threaded Drill Guides (part No. 03.503.043)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...
The Issue: Potential patient data mixup. Improper error handling could allow for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...
The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...
The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...
The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement Recalled by Remel Inc Due to The...
The Issue: The product may contain high levels of microbial contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.