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.
Reported Nov 19, 2014
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Prescription eyeglass safety lenses. Vision correction
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eyemart Express Ltd.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Strawberry flavored gelatin mix desert
Moderate riskThis product could cause temporary or reversible health problems — stop using it.U.B.C Food Distributors, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 5, 2014
Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Family Dollar Stores - NC Distribution Center
FDA (openFDA food enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Frozen battered onion rings packaged in 40 oz plastic bags, 6/case under the following private labels: (1) Imperial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 29, 2014
Symbia E is a multi-purpose SPECT system ideal for hospitals and outpatient centers. It is used to detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2014
GE Healthcare Carescape Patient Data Module
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
4C GRATED CHEESE HOMESTYLE 100% NATURAL PARMESAN, NET WT. 6 OZ. (170g) glass jars, UPC Number:0-41387-32790-8.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.4 C Foods, Corp.
FDA (openFDA food enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc./d.b.a.Basic American Metal Products
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 17, 2014
The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
ORGANIC TRADITIONS SPROUTED CHIA SEED POWDER NET WT. 8 oz. and 16 oz., UPC 854260006162, item number AHM616 and UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Health Matters America Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 3, 2014
Verigene CYP2C19 Nucleic Acid Test (CYP2C19 Test). Each CYP2C19 kit consists of 20 Verigene CYP2C19 Nucleic Acid Test…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nanosphere, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Organic Carob Powder, Net Wt. 55lbs (25kg), Product Code: CAROB-100
High riskUsing this product could cause serious injury, illness or death — stop using it now.BrandStorm Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
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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.