The Recall Desk

State

North Dakota product recalls

72,969 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,921
Critical
265
Severe
727
Most recent
2026-09-02

Of the 2,921 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 727 (25%) are Severe.

These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5551–5575 of 75890

  • LowFDA (Devices)·Z-2374-2025·2025-09-03

    L12-4 Lumify transducer probes recalled to clarify device useful life

    L12-4 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    L12-4 Lumify Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2385-2025·2025-09-03

    Mini Multi TEE transducer probes recalled to clarify useful life labelling

    Mini Multi TEE Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    Mini Multi TEE Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2414-2025·2025-09-03

    XL14-3 ultrasound transducer probes recalled to add useful life labelling

    XL14-3 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    XL14-3 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2395-2025·2025-09-03

    S7-3t ultrasound transducer probes recalled to add useful life labelling

    S7-3t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    S7-3t Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2409-2025·2025-09-03

    X5-1c transducer probes recalled to clarify useful life in the field

    X5-1c Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    X5-1c Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2401-2025·2025-09-03

    C10-3v transducer probe serial B2WXV7 recalled over useful life labelling

    The C10-3v Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    Transducer C10-3v Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2379-2025·2025-09-03

    L17-5 ultrasound transducer probes recalled to add useful life labelling

    L17-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    L17-5 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2360-2025·2025-09-03

    C9-2 transducer probes recalled to clarify useful life in the field

    C9-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    C9-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2354-2025·2025-09-03

    C5-2 Lumify transducer probes recalled to add useful life labelling

    C5-2 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    C5-2 Lumify Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2402-2025·2025-09-03

    L12-5 transducer probe serial B1D3VM recalled over useful life labelling

    The L12-5 Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    TRANSDUCER L12-5 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2399-2025·2025-09-03

    S9-2 transducer probes recalled to clarify useful life in the field

    S9-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.

    Product
    S9-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V569000·2025-09-02

    Kenworth trucks display system may fail to show critical warnings

    PACCAR is recalling Kenworth T680, T880, and W990 trucks from 2024–2026 because the 15-inch digital display may fail to show warning lights or vehicle speed, increasing crash risk.

    Product
    KENWORTH — KENWORTH T680, T880, W990
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V568000·2025-09-02

    2025 Mazda CX-90: Inaccurate Fuel Gauge May Cause Unexpected Stalling

    Mazda is recalling certain 2025 Mazda CX-90 vehicles (also 2024 CX-90 and 2025 CX-70 mild hybrid models) because the fuel gauge may display an inaccurate reading, which could cause unexpected stalling and increase crash risk.

    Product
    MAZDA — MAZDA CX-70, CX-90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V566000·2025-08-29

    New Flyer Recalls Electric Buses Due to Battery Overheating Risk

    New Flyer is recalling specific electric bus models because an inadequate weld and software error may cause battery modules to overheat, increasing the risk of fire.

    Product
    NEW FLYER — NEW FLYER XHE40, XE40, XE35, XE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V562000·2025-08-29

    Altec utility vehicle cable entry steps can detach during use

    Altec is recalling certain 2011-2025 Aerial Device, Digger Derrick and Service Body vehicles because the cable step wire rope assembly may be improperly secured, allowing the entry step to detach.

    Product
    ALTEC — ALTEC, TEREX AERIAL DEVICE, DIGGER DERRICK, SERVICE BODY, AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V560000·2025-08-29

    Fontaine Recalls 2025-2026 Forklift Trailers Due to Brake System Defect

    Fontaine Trailer Company is recalling 2025-2026 forklift trailers because misinstalled cables may disable the anti-lock brake system, increasing crash risk.

    Product
    FONTAINE — FONTAINE FORKLIFT TRAILER HCIFL82CTA, FORKLIFT TRAILER HCIFL12SAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V567000·2025-08-29

    MCI Recalls Electric Buses Due to Battery Overheating and Fire Risk

    Motor Coach Industries is recalling specific 2020-2025 electric buses because an inadequate weld and software error may cause battery overheating and fire.

    Product
    MCI — MCI D45CRTELE, J4500E, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide