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 Feb 17, 2016
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Dental Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 129602 Distributed by: Solstice…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison One Acme Inc.
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by Mars Chocolate na, llc Hackettstown, NJ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mars Chocolate North America
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resmed Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2016
This Kid Saves Lives Chocolate Chip UPC #10858497004097 UPC# 858497004090
Moderate riskThis product could cause temporary or reversible health problems — stop using it.This Bar Saves Lives
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Zatarain's New Orleans Style RED BEANS AND RICE, ORIGINAL, NET WT 8 OZ, UPC 7142909849
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zatarain's Partnership, LP
FDA (openFDA food enforcement)
Reported Feb 3, 2016
Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midmark Corp. dba Progeny Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2016
TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY. Indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abeon Medical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Healthcare
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Friendly Farms Greek Peach Parfait Nonfat Yogurt net wt. 5.3 oz (150g) Distributed by ALDI Inc., Batavia, IL 60510
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ehrmann Arizona Dairy LLC
FDA (openFDA food enforcement)
Reported Jan 6, 2016
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Vancomycin Screen Agar
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
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.