All recall categories

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.

Medical devices

Reported Jun 20, 2018

Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Keystone Dental Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

New Century Snacks LLC

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2018

Commercial breaders and batters Product B58042 Breader XI- 50 pound bags Product B58915 Breader X1- 40 pound bags…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Newly Weds Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Desly International Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Renal Therapies Group, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lake Michigan Distilling Co. LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Restoris MCK Onlay Insert Extractor.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Orthofix, Inc.

19 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 6, 2018

Alfalfa Seeds

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Caudill Sprouting LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 6, 2018

Carina Ventilator, ventilator. Catalog no. 5704110. Long-term ventilator for treatment in hospitals by a qualified…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Gyrus Acmi, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Maquet Datascope Corp. - Cardiac Assist Division

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 6, 2018

Terry's Potato Salad, Packaged into the following sized containers: 1. Net Wt. 30 lbs. (13.68kg), Mfg No. 20117, UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Morski Brands Inc. dba Dawn's Fresh Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 6, 2018

MagNA Pure 24 System, GMMI: 07290519001 Product Usage: The MagNA Pure 24 System is a fully automated clinical sample…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Molecular Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Torax Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

WRP Asia Pacific Sdn Bhd

FDA (openFDA device enforcement)

Food

Reported Jun 6, 2018

Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Ziyad Brothers Importing, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 30, 2018

Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LivaNova USA

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Madison Polymeric Engineering

5 more products in this recall

FDA (openFDA device 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.