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.

Which agencies issued them

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.

5426–5450 of 73353

  • ModerateFDA (Devices)·Z-2453-2025·2025-09-03

    Drug transfer devices recalled for shipping without US instructions for use

    BD PhaSeal closed system drug transfer devices are recalled because they were shipped to the US market without a US version of the instructions for use. 3,884,670 units are affected.

    Product
    BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD PhaSeal Injector Lu63er Lock (N35C Multi), REF: 515005 BD PhaSeal Protector (P14), REF: 515100 BD PhaSeal Protector (P21), REF:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2418-2025·2025-09-03

    NovoTHOR Gen 3.0 unit recalled because gas strut may detach from canopy

    A single NovoTHOR Gen 3.0 Reg PRX unit, model S2189, is recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift.

    Product
    Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissu
    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-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-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-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-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-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-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-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
  • 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-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-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-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-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