The Recall Desk

State

North Dakota product recalls

73,596 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,925
Critical
265
Severe
869
Most recent
2026-10-14

Of the 2,925 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 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,925 recalls whose distribution notice names North Dakota specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27201–27225 of 76521

  • HighFDA (Devices)·Z-0896-2021·2021-02-03

    Philips Respironics V60 Plus Ventilator Recalled for Backup Battery Failure

    Respironics is recalling 3,887 V60 Plus Ventilators because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 481 V60 Ventilators due to potential backup battery failures caused by over-discharge or extended storage without AC power.

    Product
    Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 534 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.

    Product
    Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0913-2021·2021-02-03

    Philips Respironics V60 Plus Ventilator Recall Due to Navigation Ring Malfunction

    The FDA is recalling the Philips Respironics V60 Plus Ventilator because its navigation ring may become inoperative or operate intermittently, potentially causing ventilator parameter values to change erratically during setup or adjustment.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2021·2021-02-03

    Philips Respironics V60 Plus Ventilator Recalled for Battery Failure Risk

    Respironics is recalling 702 V60 Plus Ventilators worldwide because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V045000·2021-02-03

    Royal Enfield Recalls 2018-2020 Motorcycles for Brake Caliper Corrosion

    Royal Enfield is recalling 2018-2020 Continental GT 650 and Interceptor 650 motorcycles because road salt may corrode brake calipers, potentially reducing braking performance.

    Product
    ROYAL ENFIELD — ROYAL ENFIELD CONTINENTAL GT 650, INTERCEPTOR 650
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E008000·2021-02-03

    Bigfoot Truck Campers Recalled for Potential Gas Leak Risk

    Bigfoot Industries is recalling specific 1500 and 2500 Series truck campers because a saddle valve bolt may be overtightened, damaging the seal and causing a gas leak that increases fire risk.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0912-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 216 V60 Ventilators because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0902-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 2,137 V60 Ventilators because the navigation ring may malfunction or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0917-2021·2021-02-03

    Philips Respironics V680 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 3,453 V680 ventilators worldwide because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 3,213 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0908-2021·2021-02-03

    Philips Respironics V60 Ventilator Recall for Navigation Ring Issues

    Respironics is recalling 3,752 V60 Ventilators worldwide due to potential navigation ring malfunctions that may cause erratic parameter changes or inoperability.

    Product
    Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2020·2021-02-03

    Philips Telemetry Transceiver Recall for Heart Rate Display Failure

    Philips is recalling 21,672 telemetry transceivers because they may fail to display heart rates or generate alarms when used with specific Patient Information Center software.

    Product
    TRx4851A 2.4 GHz IntelliVue Tele TRX, Model Number 862231; Includes Service Numbers 453564052401, 453564052411, 453564052441, 453564052451, 453564166851, 453564166861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0918-2021·2021-02-03

    Fujifilm Synapse PACS Software Recalled for Clinical Reporting Errors

    Fujifilm Medical Systems is recalling Synapse PACS Software versions 7.0.0 and 7.0.1 because the software fails to update measurements when ventricular traces are changed by different users.

    Product
    FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Usage: intended for use as a web based application on an off-the shelf PC which meets or exceeds minimum specifications and is networked with a FUJIFILM Synapse PACS server.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0242-2021·2021-02-03

    Good & Gather Four Cheese Gnocchi Recalled for Foreign Material

    EMILIA FOODS SRL is recalling Good & Gather Four Cheese Gnocchi because the product may contain foreign material.

    Product
    Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1 Product of Italy. Dist by Target Corporation, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0930-2021·2021-02-03

    B. Braun Introcan IV Safety Catheters Recalled for Lack of FDA Approval

    Braxton Medical Corporation is recalling B. Braun Introcan IV Safety Catheters because the products do not have FDA approval for sale in the United States.

    Product
    B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0865-2021·2021-02-03

    Nihon Kohden PSG-1100 Sleep Diagnostic System Recalled for Electrical Safety Non-Conformance

    Nihon Kohden America Inc is recalling 189 PSG-1100 Sleep Diagnostic Systems because they do not meet the IEC 60601-1 electrical safety standard.

    Product
    PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI (01) 04931921108383; Made in Japan The PSG-1100 Sleep Diagnostic System is a digital PSG amplifier intended to record the electrical activity of the brain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0932-2021·2021-02-03

    Fujifilm Recalls Wako HDL-C/LDL-C Calibrator Due to Labeling Error

    Fujifilm is recalling Wako HDL-C/LDL-C Calibrator Lot EL629 because incorrect concentration values were printed on the bottle labels, which may result in incorrect testing results.

    Product
    Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used with Wako L-Type HDL-C or L-Type LDL-C for the determination of high density lipoprotein cholesterol (HDL-C) or low density lipoprotein cholesterol (LDL-C) in serum or plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0727-2021·2021-02-03

    Philips ProxiDiagnost N90 X-ray System Recalled for Software Lock-in Defect

    Philips is recalling 91 ProxiDiagnost N90 X-ray systems because kV and mA values may not lock correctly after a command, potentially affecting image quality.

    Product
    ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0931-2021·2021-02-03

    Yukon polyaxial screw component recalled for incorrect laser marking

    The Yukon polyaxial screw component in the Yukon Spinal System was recalled because it was incorrectly laser marked with wrong dimensions.

    Product
    Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0243-2021·2021-02-03

    Bausch Health Recalls Mephyton Tablets Due to Impurity D Failure

    Bausch Health is recalling 895 bottles of Mephyton (phytonadione) 5mg tablets because Impurity D failed stability testing specifications.

    Product
    Mephyton (phytonadione) Tablets 5mg, 100-count bottle, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC Bridgewater, NJ 08807 USA NDC 0187-1704-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0244-2021·2021-02-03

    Bausch Health Recalls Phytonadione Tablets Due to Impurity D

    Bausch Health is recalling Phytonadione Tablets 5mg because Impurity D exceeded specifications during stability testing. The recall covers 14,089 bottles distributed nationwide.

    Product
    Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA NDC 68682-170-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V041000·2021-02-02

    Shyft Group Recalls 2020-2021 Spartan K2, K3, K4 RV Chassis

    Shyft Group is recalling 2020-2021 Spartan K2, K3, and K4 RV chassis because steering gear mounting fasteners may come loose, potentially interfering with steering components and increasing crash risk.

    Product
    SPARTAN — SPARTAN K3, K4, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E007000·2021-02-01

    Howmet Aerospace Recalls Alcoa High Polish Aluminum Wheels

    Howmet Aerospace is recalling specific Alcoa High Polish Aluminum Wheels that may bend or break under load, increasing the risk of a crash.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide