The Recall Desk

State

Hawaii product recalls

72,971 recalls have nationwide distribution and so reach Hawaii. 2,767 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total
2,767
Critical
333
Severe
567
Most recent
2026-09-16

Of the 2,767 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (20%) are Severe.

These figures cover only the 2,767 recalls whose distribution notice names Hawaii specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5576–5600 of 75738

  • 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-2381-2025·2025-09-03

    L8-4 transducer probes recalled to add field useful life labelling

    L8-4 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
    L8-4 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2348-2025·2025-09-03

    7.5 MHz Endo transducer probes recalled to clarify useful life labelling

    The 7.5 MHz Endo 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
    7.5MHZ Endo 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
  • LowFDA (Devices)·Z-2404-2025·2025-09-03

    V9-2 transducer probes recalled to add useful life labelling

    V9-2 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
    V9-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2391-2025·2025-09-03

    S4-1 transducer probes recalled for useful life labelling in the field

    S4-1 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
    S4-1 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2397-2025·2025-09-03

    S8-3 ultrasound probes recalled to add field useful life labelling

    S8-3 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
    S8-3 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2463-2025·2025-09-03

    Leg massagers recalled over documentation error and misleading color packaging claim

    HoMedics Air Compression Leg Massagers, model SR-160HJ, are recalled for a regulatory documentation error and a misleading color packaging claim. The record states the affected lots do not present a risk of harm.

    Product
    Brand Name: HOMEDICS Product Name: Air Compression Leg Massager Model/Catalog Number: SR-160HJ Product Description: Powered Inflatable Tube Massager used on the leg. The Air Compression Leg Massager is indicated for the temporary relief of minor muscle aches and pains and f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2346-2025·2025-09-03

    3D6-2 transducer probes recalled to add field useful life labelling

    3D6-2 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
    3D6-2 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-90, CX-70
    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 W990, T680, T880
    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 HCIFL12SAT, FORKLIFT TRAILER HCIFL82CTA
    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·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 XE40, XE60, XHE60, XE35
    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
  • 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 EAGLE, AMERICAN TRADITION, AMERICAN DREAM, PALISADE
    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
  • 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