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 26, 2017
Code: LM290; Keep Frozen; Lucky's Maryland Style Crab Cakes: Net Wt. 13.5 lbs; 72-3OZ; packed for Lucky's Markets,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wicks
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 19, 2017
VIDAS Testosterone, Ref 30418
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CryoLife, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 19, 2017
The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
The Smokehouse of NY Smoked Norwegian Fish packaged as: 4oz & 8oz and whole sides
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Smokehouse
FDA (openFDA food enforcement)
Reported Jul 12, 2017
CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measurement system used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CardioTek BV
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Logic Fit Tibial Tamp Head
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutri-Dyn Midwest, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Gourmet Bay - Toasted Crumb Breaded Tilapia, 5-7 oz. (Bulk 5 lbs container) refrigerated Product Code: 7396701
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Slade Gorton & Company, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 5, 2017
ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle, ROTH Catalogue Number 14002 96 S, EOS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EOS Imaging
FDA (openFDA device enforcement)
Reported Jul 5, 2017
DIASTAT(R) ANA (anti-Nuclear antibody) EURO DIAGNOSTICA, The DIASTAT(R) anti-nuclear antibody (ANA) test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Euro Diagnostica AB
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Exactech 1.5" Novation Calcar Planer Guide Tip To assist the surgeon in the implantation of Novation hip system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2017
Vinh Hoan USA, Inc. Recalls Siluriformes Fish Products Due To Failure To Comply With FSIS Import Requirements
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vinh Hoan USA, Inc.
USDA FSIS
Reported Jun 21, 2017
Chocolate chip cookie dough larabars, 10 count , UPC 100-21908-49031 incorrectly packaged in peanut butter cookie…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
CADD¿ High Volume Administration Set with FlowStop, 21-7381-24. Product Usage: The CADD¿ High-Volume Administration set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Arsenal Spinal Fixation System, Set Screw, Part No. 47027 Product Usage: The Arsenal Spinal Fixation System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
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.