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.

53,342 total recalls
2,520 in last 12 months

Showing 2916129180 of 53,342 recalls

FoodOctober 6, 2017· Champion Foods, LLC

Recalled Item: Little Caesar's Family Meal Kits Recalled by Champion Foods, LLC Due to...

The Issue: Champion Foods, LLC is voluntarily conducting a recall of multiple brands of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· Kiriko, LLC.

Recalled Item: A1 Slim Recalled by Kiriko, LLC. Due to Undeclared Sibutramine

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· AVKARE Inc.

Recalled Item: Duloxetine Delayed-release Capsules USP Recalled by AVKARE Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: slightly elevated levels of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Monteris Medical Corp

Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...

The Issue: The firm received complaints that involved an unanticipated interaction...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...

The Issue: While reviewing documentation for the next software release of the 2008T, an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...

The Issue: Firewall installed with Philips IntelliVue Information Center iX or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Teleflex Medical

Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...

The Issue: The product has a non-conformity that may cause clips to mislead, jam or...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...

The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund