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. 1,108 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,108 in last 12 months

Showing 7141–7160 of 29,286 recalls

Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball bearings...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Mobius Imaging, LLC

Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...

The Issue: Stryker received one report of an injury to an untrained user that occurred...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CENTRAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE LCPH LAB DRAW KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CHEST...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ANGIO PORT KIT W/HIGH GRADE IN...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Trilogy 100 Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS IR...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE HAND PACK Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PLASTICS/PEDS KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE PERF. ASSOC. CUT DOWN TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Adult Craniotome Intended for cutting and shaping bone Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing