The Recall Desk

State

North Dakota product recalls

73,092 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
729
Most recent
2026-09-23

Of the 2,924 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 729 (25%) are Severe.

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9701–9725 of 76016

  • HighNHTSA·24V722000·2024-09-27

    Forest River Recalls 2024-2025 Viking and Clipper Trailers for Lighting Defect

    Forest River is recalling 2024-2025 Viking and Clipper travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.

    Product
    FOREST RIVER — FOREST RIVER, VIKING TRAVEL TRAILERS CLIPPER CAMPING TRAILER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V725000·2024-09-27

    Ford stripped chassis gear position indicator may not display properly

    Ford is recalling certain 2024 F-53 and F-59 stripped chassis vehicles because the instrument panel cluster may not properly display the transmission gear position indicator, failing FMVSS 102.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V713000·2024-09-27

    Royal Enfield motorcycles have insufficient side and rear reflectors

    Royal Enfield is recalling certain 2023 Himalayan, Classic 350, Meteor 350, Hunter 350, Super Meteor 650, Int 650 and Continental GT 650 motorcycles whose side and rear reflectors fail FMVSS 108.

    Product
    ROYAL ENFIELD — ROYAL ENFIELD SUPER METEOR 650, CLASSIC 350, HIMALAYAN, HUNTER 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24377·2024-09-26

    John Deere Compact Utility Tractors Recalled for Brake Failure Hazard

    Deere & Company is recalling about 147,900 John Deere 1023E, 1025R, and 2025R Compact Utility Tractors because the front bell crank in the brake linkage can fail, causing loss of braking and crash risk. Four failures have been reported, including one hospitalization and two impact injuries.

    Product
    John Deere 1023E, 1025R, and 2025R Compact Utility Tractors
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V717000·2024-09-26

    Brinkley Model Z safety chains are underrated for the weight rating

    Brinkley RV is recalling certain 2025 Model Z travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating. 40 units are affected.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V718000·2024-09-26

    Tesla Cybertruck rearview camera image may be delayed after shifting

    Tesla is recalling certain 2024 Cybertruck vehicles because the rearview camera image may be delayed after shifting into reverse, failing FMVSS 111. 27,185 units affected.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V719000·2024-09-26

    Harley-Davidson Recalls 2018-2019 Softail Motorcycles for Tire Label Error

    Harley-Davidson is recalling 2018-2019 Softail FXBB and FXLR motorcycles because the front tire inflation pressure on the VIN label may be incorrect, potentially leading to tire overloading.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXBB, FXLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V715000·2024-09-26

    Chrysler Recalls 2024 Ram Promaster BEV for Software Defect

    Chrysler is recalling 2024 Ram Promaster BEV vehicles because incorrect software may cause a loss of drive power, increasing crash risk.

    Product
    RAM — RAM PROMASTER BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24378·2024-09-26

    Liberty Hardware Multi-Grip Tub Safety Bars Recalled for Fall Hazard

    Liberty Hardware is recalling about 174,500 Multi-Grip Tub Safety Bars because plastic grip pads can become dislodged on tapered tubs, making the bars unstable and creating a fall hazard. One minor fall injury has been reported.

    Product
    Multi-Grip Tub Safety Bars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V714000·2024-09-25

    BMW Recalls 2024-2025 Models Due to Steering Spindle Breakage Risk

    BMW is recalling specific 2024-2025 models because the steering spindle may break, increasing steering effort and crash risk. Dealers will replace the joint free of charge.

    Product
    BMW — BMW I5 EDRIVE40, 540I XDRIVE, 760I XDRIVE, 530I XDRIVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V711000·2024-09-25

    BMW and MINI front body structure bolts may not be tightened

    BMW is recalling certain 2023-2024 228i, 228i xDrive and 2025 MINI Countryman S ALL4 vehicles because the bolts connecting the front body structure to the chassis may be loose.

    Product
    BMW — BMW, MINI 228I XDRIVE, 228I, COUNTRYMAN S ALL4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1809-2024·2024-09-25

    Bliss Tree Millet Butter Murukku Recalled for Undeclared Sesame and Milk Allergens

    Bliss Tree Millet Butter Murukku products are being recalled due to undeclared sesame and milk allergens. Affected products were distributed to retailers and online customers in multiple states.

    Product
    Bliss Tree Millet Butter Murukku 200g UPC:8906087451631. Packaged in box, 13 boxes per cases. Bliss Tree Millet Butter Murukku 400g UPC:8906087452850. Packaged in pouches, 8 pouches per cases.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E079000·2024-09-25

    Tenneco Aftermarket Ball Joint Recall for Ford Escape Vehicles

    Tenneco is recalling aftermarket ball joints for 2013-2019 Ford Escape vehicles because they may separate, causing loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3141-2024·2024-09-25

    Alaris Syringe Module Model 8110 Infusion Pumps Recalled for Bent Connectors

    CareFusion's Alaris Syringe Module Model 8110 infusion pumps are being recalled because affected units may have bent female connectors that can prevent device operation and delay infusions. Approximately 20,145 units have been distributed worldwide.

    Product
    Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3167-2024·2024-09-25

    PHILIPS INTEGRIS X-ray systems cable hose carrier detachment recall

    PHILIPS medical X-ray imaging systems may have a cable hose carrier that can detach due to broken plastic or bolts, potentially causing parts to fall and injure clinical staff.

    Product
    System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 722021 INTEGRIS Allura 9 (biplane) 722018 Integris Allura 9 722017 Integris H5000 F / Allura 9F 722016 Integris H5000 C / Allura 9C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3140-2024·2024-09-25

    Alaris EtCO2 Module Model 8300 Recalled Due to Bent Connector

    CareFusion 303, Inc. recalls 180 Alaris EtCO2 Module Model 8300 units with potentially bent female connectors that may prevent device operation, risking delays in infusion and monitoring.

    Product
    Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3145-2024·2024-09-25

    GE Healthcare ViewPoint Imaging System Recall for Data Vulnerability

    GE Healthcare is recalling three ViewPoint imaging systems due to a software vulnerability in Mirth Connect that could allow unauthorized access and manipulation of patient data.

    Product
    ViewPoint; system, imaging processing, radiological
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1808-2024·2024-09-25

    Bliss Tree Ragi Butter Murukku recalled for undeclared milk allergen

    Bliss Tree Ragi Butter Murukku 200g and 400g packages are recalled due to undeclared milk. Consumers with milk allergies should not consume these products and contact their retailer.

    Product
    Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packaged in a box, 13 boxes per case Bliss Tree Ragi Butter Murukku 400g UPC:8906087452829. Packaged in a pouch, 8 pouches per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3170-2024·2024-09-25

    Diagnostic test reagent may produce inaccurately low patient results

    Siemens Healthcare's ADVIA Chemistry Microalbumin diagnostic test may produce falsely low results. Eight lots do not meet High-Dose Hook Effect and Prozone Effect specifications, potentially affecting microalbumin detection accuracy.

    Product
    ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in the quantitative measurement of microalbumin in human urine on ADVIA Chemistry systems/ Atellica CH and Atellica CI Analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3155-2024·2024-09-25

    Shoulder implant recalled due to excessive bacterial endotoxin

    Tornier, Inc. is recalling one lot of the Stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS shoulder implant due to bacterial endotoxin exceeding safety specifications. The 5 affected units were distributed in Illinois, Wisconsin, Arizona, Nevada, and South Dakota.

    Product
    stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus, REF DWM003A; anatomic total arthroplasty of the shoulder
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3174-2024·2024-09-25

    Hemodialysis tubing may fail to flow if connector is incompletely inserted

    B Braun's STREAMLINE FRESENIUS bloodline tubing used in hemodialysis may have a design issue where incomplete insertion of the patient connector prevents proper blood flow during certain procedures. Patients receiving dialysis may experience treatment delays.

    Product
    STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3177-2024·2024-09-25

    Hemodialysis tubing connector may not fully insert, risking flow occlusion

    B. Braun Medical is recalling STREAMLINE LONG hemodialysis bloodline tubing because the patient connector may fail to fully insert into the Locksite, potentially causing blood flow obstruction during dialysis treatment.

    Product
    STREAMLINE LONG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095W
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3146-2024·2024-09-25

    Medical imaging systems vulnerable to unauthorized access due to software vulnerability

    GE Healthcare ViewPoint 6 medical imaging systems contain a software vulnerability (CVE-2023-43208) in Mirth Connect that could allow unauthorized access and patient data manipulation. 574 units are affected and distributed nationwide.

    Product
    ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA; system, imaging processing, radiological
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3139-2024·2024-09-25

    Alaris PCA Pump Module May Have Defective IUI Connector

    CareFusion recalls approximately 10,460 Alaris PCA Module Model 8120 infusion pumps worldwide due to potentially bent female IUI connectors that may prevent proper device operation and delay treatment initiation.

    Product
    Alaris PCA Module Model 8120, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide