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 Jul 16, 2014
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregon Freeze Dry, Inc.
FDA (openFDA food enforcement)
Reported Jul 16, 2014
PALL Medical Breathing Circuit Filter, REF BB50T and BB50T-BULK , Rx ONLY Single use, bi-directional bacterial/viral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pall Corporation
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RGI Medical Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Rosemary & Olive Oil Gluten Free Snack Crackers sold under the following brand names and sizes: 1. glutino, Net Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baptista's Bakery, Inc.
FDA (openFDA food enforcement)
Reported Jul 9, 2014
BD FACS Canto and associated Fluidics Cart Product Usage: Flow cytometer for use in In vitro Diagnostics.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BD Biosciences, Systems & Reagents
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Brunkow Cheese of Wisconsin, Monterey Jack Morel Mushroom & Onion Cheese, 5 lb block plastic wrapped and vacuum sealed.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Brunkow Cheese
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Global Cooling Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Laceration Trays, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc., Arden, NC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Ocean Spray¿ Greek Yogurt Covered Craisins¿ Dried Cranberries , 8 oz Resealable Pouch UPC: #23719
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ocean Spray Cranberries Inc.
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Sharp Cheddar Cold Pack Cheese sold under the following sizes and brands: 1. Parkers Farm or Parkers label in 8 ounce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Parkers Farm Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 9, 2014
BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Dark Old Fashioned Sponge Candy, sold under the following brand and sizes: 1. Eillien's in Net Wt. 6 oz (170g) UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eillien's Candies, Inc.
FDA (openFDA food enforcement)
Reported Jul 2, 2014
Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
44 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
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.