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 Oct 24, 2018

GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

Sweet Me Creamery Brookie Dough ice cream, packaged in following configuration: 1 Pint (473 ML), UPC: 41483-04219 or…

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

Kemps, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures

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

Zimmer Biomet, Inc.

47 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 19, 2018

Buddy's Kitchen, Inc. Recalls Pork and Chicken Products due to Possible Salmonella and Listeria monocytogenes…

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

Buddy's Kitchen, Inc.

USDA FSIS

Meat & poultry

Reported Oct 19, 2018

Caito Foods, LLC Recalls Salad And Bowl Products Made With Chicken Due To Possible Salmonella and Listeria…

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

Caito Foods, LLC

USDA FSIS

Medical devices

Reported Oct 17, 2018

Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology Suite/Cardiology Suite) when deployed as a…

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

Agfa Healthcare NV

FDA (openFDA device enforcement)

Drugs

Reported Oct 17, 2018

Thyroid powder, 4.5 kg foil bag, 5x1 kg foil bags packed in 25 Kg Fiber Drum, Thyroid Powder 25kg/drum, US…

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

Alkano Chemicals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 17, 2018

Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…

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

Bayer Medical Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Colpo-Pneumo Occluder, Part CPO-6

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Hodgson Mill Cookie Mix Gluten Free 12oz. cardboard carton retail unit; 6 retail units per case. UPC Code 0 71518 02125…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hodgson Mill Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 17, 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…

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

Neomed Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…

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

Sarap Asian Fusion

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 17, 2018

Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters into the heart. (a)…

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

Sterilmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral…

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

Stryker Spine

FDA (openFDA device enforcement)

Medical devices

Reported Oct 10, 2018

ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…

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

Endologix

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 10, 2018

Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…

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

Neighbors LLC

FDA (openFDA food enforcement)

Food

Reported Oct 10, 2018

EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…

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

Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in…

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

Agfa N.V.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

ESSENTIO Pacemaker

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

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 3, 2018

Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refrigerated. UPC 85392700334

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

Brett Anthony Foods

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…

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

GE Medical Systems, LLC

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.