Recalls distributed in Michigan
These notices name Michigan in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,580 stored notices name Michigan, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Dec 14, 2016
MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thayer Intellectual Property, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Aequalis Fx2 implant parts and instrument trays. Insert component : Part Numbers DWK204B-DWK206B, DWK224B-DWK226B,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Kuster's Dairy Foods Three Blend Shredded Cheese, 5 lb. packages packed in plastic bags, keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kuster's Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 7, 2016
MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Three Way Popcorn Sampler that contains three types of popcorn (cheese, carmel and buttered popcorn) packed inside one…
High riskUsing this product could cause serious injury, illness or death — stop using it now.JML Holdings Inc.
FDA (openFDA food enforcement)
Reported Nov 30, 2016
Merge RadSuite,f/k/a: Emageon Advanced Visualization , RadSuite versions 8.30.7.8, 8.30.7.9, 8.30.8, and 8.31. Advanced…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Simply Balanced brand White Chicken Chili dry soup mix. This is not a ready to eat product and it does not contain any…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Conifer Specialties, Inc.
FDA (openFDA food enforcement)
Reported Nov 23, 2016
White Cheddar Cheese, 40 lb. blocks
High riskUsing this product could cause serious injury, illness or death — stop using it now.Farm Country Cheese House, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.1 Epic, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 16, 2016
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Fit & Active 100 Calorie Whole Almonds 7 0.63oz bags per retail carton Flexible film bags in paperboard carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kar Nut Products Company
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 16, 2016
The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schaerer Medical USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2016
FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SentreHeart Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Solo Almond Paste, 6/7 LB. Cans, Net Weight: 42 LBS. (19.09 KG.)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sokol and Co.
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
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Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.