The Recall Desk

State

Guam product recalls

72,968 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total
385
Critical
14
Severe
37
Most recent
2026-01-28

Of the 385 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 37 (10%) are Severe.

These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5476–5500 of 73353

  • 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-2406-2025·2025-09-03

    X11-4t transducer probes recalled to add useful life labelling

    X11-4t 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
    X11-4t Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2355-2025·2025-09-03

    C6-2 ultrasound probes recalled for useful life labelling in the field

    C6-2 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
    C6-2 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-2390-2025·2025-09-03

    S3-1 transducer probes recalled over useful life labelling clarification

    S3-1 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
    S3-1 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-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-2369-2025·2025-09-03

    eL18-4 transducer probes recalled to clarify useful life labelling

    eL18-4 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
    eL18-4 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-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-2392-2025·2025-09-03

    S4-1 Lumify transducer probes recalled to define transducer useful life

    S4-1 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
    S4-1 Lumify Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2388-2025·2025-09-03

    OMNI III TEE transducer probes recalled to add useful life labelling

    OMNI III 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
    OMNI III TEE 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·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