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 Dec 19, 2012
Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Berres Brothers, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2012
Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutaneous electrode is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC dba Uni-Patch
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Novocastra Ready-to-Use Mouse Monoclonal Antibody Terminal Deoxynuceotidyl Transferase Staining Reagent; an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2012
DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA, Inc. 800 MacArthur Blvd. Mahwah, NJ 07430 USA.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Dec 19, 2012
Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are infrared LED lamps that are labeled in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc. dba Silver Bay LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Sara Lee Butter Streusel Coffee Cake, Net Wt. 11.5 oz ; 8 cakes per 5.75 lb case; Distributed by Sara Lee Corp.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hillshire Brands Company
FDA (openFDA food enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Sukhi's Gourmet Indian Food; Red Curry Vegetables; 9 oz. package. Manufactured by Jagpreet Enterprises dba Sukhi's…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jagpreet Enterprises Inc.
FDA (openFDA food enforcement)
Reported Dec 12, 2012
The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Ground limestone also known as calcium carbonate. Omya's food grade ground limestone products. All bulk with no product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Omya Inc.
FDA (openFDA food enforcement)
Reported Dec 12, 2012
Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Jimmy Dean French Toast & Sausage Sandwich, Net Wt 3.9 oz (110g); a food service individually butcher paper wrapped,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hillshire Brands Company
FDA (openFDA food enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
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 Nov 28, 2012
bioMerieux BacT/ALERT Control Module, catalog number 210147, Clinical instrument The product is most commonly used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
31 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
CapLOX II Final Torque Driver, Indicator is a Pedicle screw spinal system. The CapLOX II Spinal System is a posterior,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Captiva Spine, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovative Magnetic Resonance Imaging Systems Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Signs Devices, a GE Healthcare Company
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Peanut Butter Pave, UPC code 693868102117 & 69386905312, in the following sizes: 1) 5 Piece Peanut Butter Pave, 63…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B.T. McElrath Chocolatier, Inc.
FDA (openFDA food enforcement)
Reported Nov 21, 2012
PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical 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.