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 Nov 27, 2013
Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement of tracheal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY; Terri Lynn Inc.; Deluxe Mixed; No Peanuts; NET WT. 16 OZ.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Terri Lynn Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 20, 2013
SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
3.5MM LOCKING SCREW, T15 HEXALOBE, SELF TAPPING, 34MM The OrthoPediatrics Proximal Femur Plating System combines…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Nov 20, 2013
White grits packaged in a paper bag labeled in part: Smooth & Creamy; Aunt Jemima; Quick GRITS; Cooks in about 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quaker Foods and Snacks North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 20, 2013
Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange, angled tip, wire-reinforced with luer port, aortic cannula, 8.0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Product Usage: The TorFlex…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baylis Medical Corp. *
FDA (openFDA device enforcement)
Reported Nov 13, 2013
DRX Revolution, Catalog #'s 1)1019397, 2) 1023415 (w/ installation warranty, US-only) and 3) 1023423 (w/ parts…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz, Switzerland; Imported and distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 13, 2013
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitalab Co. Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atossa Genetics, Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2013
P.F. Chang's Home Menu, Pork & Leek Dumplings, frozen, packaged in 12.5 oz bags. UPC: 0 36200 21215 8
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare It
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
HemoCue¿ Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, Sweden The quantitative, rapid,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HemoCue AB
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 6, 2013
Breeze C Scooter is a motorized electric scooter for elderly people. Brand name Breeze, model C. It is intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.S.a.e. Afikim
FDA (openFDA device enforcement)
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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.