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. 2,716 recalls have been distributed to Michigan in the last 12 months.
Showing 5601–5620 of 29,286 recalls
Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...
The Issue: When using affected curette and software, there is a discrepancy between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...
The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists...
The Issue: Eye syncing issues causing the device to be inoperable. Unable to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit-For in vitro diagnostic use Recalled by...
The Issue: During an internal audit a small percentage (<10%) of plastic caps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System Recalled by...
The Issue: Device packaged inside an incorrect outer box; displaying artwork &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Dry Seal Chest Drains (Express): 4000-100N DRAIN Recalled by Atrium...
The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.