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 Feb 18, 2015
MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
VisiPlugST for the Lacrimal Efficiency Test. It is also sold in the EU as CollaSyn Plugs. Model number 1813, 1814,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lacrimedics Inc.
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Ground Cumin Seeds, ETO Treated, 50 lbs packaged in 50 lb brown paper bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schiff Foods Products
FDA (openFDA food enforcement)
Reported Feb 18, 2015
Hot Smoking BBQ Sauce
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Son In Law Products
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Craniomaxillofacial Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MAQUET, SERVO Humidifier 163, Rx Only, Inmed Mfg. Sdn Bhd. Catalog No: XKC01-06-8125-8, Model No. 01-06-8125-8. A heat…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex Medical
17 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex, Inc.
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Virtual Imaging, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2015
Michigan Brand, Inc. Recalls Products Due to Misbranding and an Undeclared Allergen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Michigan Brand Inc.
USDA FSIS
Reported Feb 11, 2015
Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Dried Bean Curd Satay Flavor, 24x150g, Item No. 8533.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gemini Food Corporation Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2015
ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood gases, electrolytes,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Arriba! 16 oz. Chili Con Queso-Hot; 6 units per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Riba Foods Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2015
SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCC Soft Computer
FDA (openFDA device enforcement)
Reported Feb 11, 2015
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Chopped Twix, chopped candy bars pieces packaged in 5 lb plastic white film bags, 2 bags per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tarrier Foods Corp.
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Raw Milk Cheddar Cheese, packaged in 8-oz. blocks and 5-lb. loafs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Farm Country Cheese House, Inc.
FDA (openFDA food enforcement)
Reported Feb 4, 2015
LaBree's Bakery Chocolate Chip Mini Muffins, 12 pack. Net wt. 10 oz. packaged in plastic clamshell. Frozen Product…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.LaBree's Bakery
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosensor, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Jan 28, 2015
FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aptalis Pharmatech Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,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.