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 Feb 1, 2017

Human Subclass Kit for use on the Beckman IMMAGE"/IMMAGE"800 Analyser Product Code LK009.IM This kit is intended for…

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

The Binding Site Group, Ltd.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2017

Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

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

Villa Radiology Systems LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 25, 2017

NO EGG CHOCOLATE CHIP COOKIE DOUGH 03-3014, Net Weight 30 lb (13.61 Kg) Aspen Hills, Inc. Garner, IA 50438

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

Aspen Hills, Inc.

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 25, 2017

Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…

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

Dicom Grid Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 25, 2017

Delizza Patisserie, Belgian Custard Cream Mini Eclairs, Net Wt. 420g  14.8 oz., UPC Code: 6 76670 00106 9(30 count)…

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

Poppie International Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

Biscuits & Gravy Seasoning CR/ Barrel O' Fun. Product Code: T3669. 50 lb bags

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

All American Seasonings, Inc.

25 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…

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

Brand Castle LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…

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

GE OEC Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

Stonewall Kitchen Cinnamon Apple Pancake & Waffle Mix, 16 oz. canister UPC: 711381025659 Item #: 551118

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

Stonewall Kitchen, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…

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

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 11, 2017

AMERICAN CLASSIC SUB Net Wt 6.5 oz (184g) Smoked ham, deli style bologna, hard salami with American and Swiss cheese on…

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

Eby Brown Co.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 4, 2017

Innova 2000

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

GE Healthcare, LLC

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2017

Kerry Upgrade Bio WS, Net Wt. 50 lb (22068 kg), Item 5R01451.

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

Kerry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2016

CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…

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

Accuray Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…

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

Angiodynamics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit

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

Exactech, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2016

Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…

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

Hi-Tech Pharmacal Co., Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2016

Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…

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

Medtronic Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2016

Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Loose case = 24  12 oz bottles ¿ 12 pack = 12  12 oz…

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

Samuel Adams Brewery Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2016

8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…

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

Stryker Instruments Div.

6 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.