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Recalls distributed in North Dakota

These notices name North Dakota 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.

1,377 stored notices name North Dakota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach North Dakota too — those are in the archive.

Food

Reported Feb 5, 2020

Excellent tahina (sesame tahini) 800 g and 400 g jars, UPC 6214002717420 and 6214002717413

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

Five Star Food Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Food

Reported Jan 22, 2020

13 Bean Soup Mix is sold under Bob's Red Mill brand, packaged in Form & Fill (29 oz. and 822 gram), Standup Pouch (29…

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

Bob's Red Mill Natural Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…

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

Physio-Control, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

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

Medtronic Navigation, Inc.-Littleton

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

STA UNICALIBRATOR (ref. 00675)

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

Diagnostica Stago, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2020

R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362

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

Ferris Coffee and Nut Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2020

VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

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

Mazor Robotics Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…

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

Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2019

Quantam 2000 Electrosurgical Generator, Part number 909075.

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2019

Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…

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

Frog Hollow Farm

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2019

EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2019

Tomato, Carrot, Broccoli & Snap Pea- 13 oz in clear plastic container. Brands: Crazy Fresh, Quick&Easy, or Plain Label

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

Russ Davis Wholesale, Inc.

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2019

Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…

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

Galil Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…

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

Western / Scott Fetzer Company

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 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.