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 Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Miranda, 5 lb. wrapped in paper; Vulto Creamery, Walton, NY.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tomales Bay Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2017
Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2017
MEDTECH ROSA Brain 3.0 The device is intended for the spatial positioning and orientation of instrument holders or tool…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2017
DX-D600 - DXD Imaging Package
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ikea North America Srvcs Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 12, 2017
Mobile Diagnostic X-Ray System with Digital Panel
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 5, 2017
AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 5, 2017
JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2017
Food Evolution, LLC. Recalls Chicken Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Food Evolution
USDA FSIS
Reported Apr 5, 2017
Copper wood Colby Jack Mini Horn, 4/6#
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 5, 2017
Great Midwest Applewood Smoked Gouda Cheese, approximately 6 lbs, keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Saputo Cheese USA, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 5, 2017
DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162; B/C: 59033 50162
High riskUsing this product could cause serious injury, illness or death — stop using it now.Seafood Avenue
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Strawberry Gelato, 5 Liter, 1 unit/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dolce Dolci LLC dba Villa Dolce Gelato
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Hitachi Oasis MRI System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Raindrop Near Vision Inlay, Model# RD1-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Revision Optics Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Sargento Ultra Thin Sliced Longhorn Colby, 6.84 oz., UPC 4610000228, with Sell By dates of 12APR17B, 02FEB17F,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sargento Foods, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
ADVIA Centaur XPT System Software Versions V1.0.1, V1.0.2, V1.0.3, V1.1 and V1.2. The ADVIA Centaur XPT System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanley Security Solutions Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Veggie Noodle Co. Butternut Spirals in 10.7 ounce clear plastic containers, UPC: 852287006059 Manufactured By Veggie…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Veggie Noodle Co.
FDA (openFDA food enforcement)
Reported Mar 22, 2017
Cedar Crest Chocolate Chip Cookie Dough Ice Cream packaged in the following sizes: Pint, 1.5 Quarts, and 3 Gallon
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cedar Crest Specialties, Inc.
2 more products in this recall
FDA (openFDA food 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.