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.
1,398 stored notices name North Dakota, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach North Dakota too — those are in the archive.
Reported May 20, 2020
Arterial Line Kit 20ga X 3", Model 498411B, Rx Only, Sterile EO, UDI: 00886333215652 - Product Usage: Arterial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported May 20, 2020
DeRoyal Sterile Custom Kits packaged as a Piggy Back with the BD PosiFlush SF Saline Flush Syringe, labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
Dole "Classic Kit Light Cesar" fresh salad mix. Salad and topping Net Wt.7.7 OZ (218g), Dressing Net 2.2 FL OZ (65ml),…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 13, 2020
REF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
TCM4 Base unit, Ref 391-880, UDI:(01)05700693918808, used with the monitor modules TCM4 (902-778), TCM40 (902-778,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Canon Aquilion Lightning, Model TSX-036A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2020
LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
32 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.James Leckey Design Ltd.
FDA (openFDA device enforcement)
Reported Apr 15, 2020
ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Nature's Blend Folic Acid 1000 mcg Dietary Supplement, 1000-count bottle, Product Number: 1280, UPC 0-79854-51280-9
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.National Vitamin Company Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Philips V60 Ventilators with Power Management PCBA part number 1055906
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical, LLC
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2020
NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087562088, Packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diabetes Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2020
Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new North Dakota recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.