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 Mar 11, 2015
KimVent Closed Suction System for Adults, Double Swivel Elbow, 12 Fr., Sterile, Distributed by Kimberly Clark Global…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Brainlab Offset Cup Impactor Universal. Part of the Brainlab hip system. An intraoperative image-guided…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Mar 4, 2015
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
FDA (openFDA device enforcement)
Reported Mar 4, 2015
HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Fruitful Juice Products Bloody Mary Beverage Concentrate with Jalapeno Flavor; Contains 59% Juice; 2 + 1 packed in 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Damon Industries
6 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
Precise Digital Accelerator Intended to be used for radiation therapy treatments of malignant neoplastic diseases, as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 18, 2015
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
FDA (openFDA device enforcement)
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
Twix Bismark. This is not a packaged item. Twix Bismarcks are produced daily to be sold in bakery display cases at…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Northern Tier Bakery (dba\ Super Mom's)
FDA (openFDA food enforcement)
Reported Feb 18, 2015
ACUSON S2000 Automated Breast Volume Scanner (ABVS), model number 10434730. The affected sub-components are #10434968 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device 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
Amana Dinner Rolls, packaged in 1 lb 2 oz plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Jefferson Street Bakery Inc.
FDA (openFDA food 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
DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Express Diagnostics Int'l., Inc.
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
High Road Craft Ice Cream & Sorbet, Limoncello Sorbet, packed in 4.9L (1.3 gallon) tubs, Manufactured by: High Road…
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Road Craft Ice Cream, Inc.
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)
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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.