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 Sep 2, 2015
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly…
High riskUsing this product could cause serious injury, illness or death — stop using it now.It Takes A Village Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
Kenosha Beef Recalls Pork Sausage Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kenosha Beef International Ltd.
USDA FSIS
Reported Sep 2, 2015
Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 Product Usage: The DigitalDiagnost…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Sep 2, 2015
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Biomedical Solutions LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Getinge 86 Series Washer/Disinfector with G1 control system software, Model 8666 and Model 8668. For use in healthcare…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Getinge Disinfection Ab
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Frozen Jamba, Fruit & Veggie Smoothies, Green Fusion, Green Apple, Mango, Pineapple, Kiwi, Banana, Broccoli and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inventure Foods
64 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Dijon Mustard Potato Salad, NET WT 3 LB (1.36 kg)
High riskUsing this product could cause serious injury, illness or death — stop using it now.D & D Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mason Vitamins, Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2015
Danish Rolls, 4 Ct., Net Wt. 13oz. in clear plastic clam shell.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Supervalu, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 12, 2015
18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Blow bags included Product Usage: The Breath Alcohol Detector…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Acon Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Paragon Laboratory Management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Technologies, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Invivo Expression MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2015
ANSPACH - Fluted Drum, Side Cut only 10MM x 14MM , REF L-10DRC-G1 Cutting shaping bone including spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
33 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2015
Land O'Frost Recalls Sausage Product Due to Misbranding
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Land O' Frost
USDA FSIS
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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.