Recalls distributed in Minnesota
These notices name Minnesota 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.
3,845 stored notices name Minnesota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.
Reported May 22, 2013
DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported May 22, 2013
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
Heartland Gourmet Gluten Free double chocolate cookie mix, DAIRY FREE, packaged in 16-oz. boxes. Manufactured by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartland Gourmet, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 22, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heartware Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 8, 2013
Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries Model number: HT70 and HT70 Plus. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Newport Medical Instruments Inc.
FDA (openFDA device enforcement)
Reported May 1, 2013
Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stellate Systems
FDA (openFDA device enforcement)
Reported Apr 24, 2013
ACIST Medical Systems Inc. The ACIST Angiographic Injection System is intended to be used for the controlled infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acist Medical Systems
FDA (openFDA device enforcement)
Reported Apr 24, 2013
EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Metal cans; labeled as containing 29 oz of pinto beans packed in water and salt
Moderate riskThis product could cause temporary or reversible health problems — stop using it.La Preferida Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2013
Intellispace Portal (ISP) Philips Medical Systems (Cleveland), Inc., IntelliSpace Portal (ISP) is a multimodality (CT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Vitrea CT Multi-Chamber Cardiac Functional Analysis application on Vitrea version 5.2 (Vitrea Enterprise Suite 1.3 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Images, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lighthouse For The Blind
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2013
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Chapter, Inc.
FDA (openFDA food enforcement)
Reported Apr 17, 2013
Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Flexible Grip which is part of the Synthes Universal Nail System. Indicated for the conventional (non-locking)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermo Fisher Scientific (Asheville) LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2013
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Torrent" irrigation tubing. Product Usage: The Torrent irrigation system (tubing and accessories to accommodate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Animas Corporation
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.