The Recall Desk

State

Colorado product recalls

72,969 recalls have nationwide distribution and so reach Colorado. 6,941 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,941
Critical
1,218
Severe
1,507
Most recent
2026-09-09

Of the 6,941 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,507 (22%) are Severe.

These figures cover only the 6,941 recalls whose distribution notice names Colorado specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5776–5800 of 79910

  • LowFDA (Devices)·Z-2375-2025·2025-09-03

    L12-5 38mm transducer probes recalled to add useful life labelling

    L12-5 38mm 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
    L12-5 38mm Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2366-2025·2025-09-03

    D2cwc transducer probes recalled to add useful life labelling

    D2cwc 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
    D2cwc 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-2356-2025·2025-09-03

    C6-3 transducer probes recalled for useful life labelling in the field

    C6-3 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
    C6-3 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
  • LowFDA (Devices)·Z-2358-2025·2025-09-03

    C8-4v ultrasound transducer probes recalled to add useful life labelling

    C8-4v 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
    C8-4v Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2411-2025·2025-09-03

    X7-2 transducer probes recalled over useful life labelling clarification

    X7-2 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
    X7-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2394-2025·2025-09-03

    S5-2 transducer probes recalled to add useful life labelling

    S5-2 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
    S5-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2403-2025·2025-09-03

    V6-2 transducer probes recalled to clarify useful life in the field

    V6-2 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
    V6-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2389-2025·2025-09-03

    S12-4 transducer probes recalled to clarify useful life in the field

    S12-4 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
    S12-4 Transducer Probe
    Category
    Medical Device
    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
  • 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
  • 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
  • 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
  • HighNHTSA·25V565000·2025-08-29

    Motorhome waste tank macerator fuse can overheat and melt housing

    REV Recreation Group is recalling certain American Coach, American Eagle, American Dream and Fleetwood Palisade RVs because the waste tank macerator fuse may overheat and melt the fuse housing.

    Product
    AMERICAN COACH — AMERICAN COACH, FLEETWOOD AMERICAN DREAM, PALISADE, AMERICAN EAGLE, AMERICAN TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V564000·2025-08-29

    Tuff Trailer USA Recalls 2024 TTA17200T and TTA18200T Trailers

    Tuff Trailer USA is recalling 2024 TTA17200T and TTA18200T trailers because incorrect GVWR labels may lead to overloading and coupler failure.

    Product
    TUFF TRAILER USA — TUFF TRAILER USA TTA17200T, TTA18200T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E053000·2025-08-29

    Hiab Recalls Specific Reverse Hoists Due to Mounting Pin Failure Risk

    Hiab USA Inc. is recalling specific Galfab reverse hoists because a mounting pin may fail, allowing the hoist to fall and increasing the risk of injury.

    Product
    EQUIPMENT:MECHANICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide