The Recall Desk

State

Indiana product recalls

72,966 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,556
Critical
1,903
Severe
2,136
Most recent
2026-09-16

Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.

These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5801–5825 of 82522

  • 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-2378-2025·2025-09-03

    L15-7IO transducer probe serial B1K740 recalled over useful life labelling

    The L15-7IO 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
    L15-7IO TRANSDUCER 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
  • 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-2386-2025·2025-09-03

    mL26-8 transducer probes recalled to add field useful life labelling

    mL26-8 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
    mL26-8 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-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-2364-2025·2025-09-03

    C9-4v transducer probes recalled for useful life labelling clarification

    C9-4v 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
    C9-4v 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-2352-2025·2025-09-03

    c5-1 transducer probes recalled for useful life labelling in the field

    c5-1 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
    c5-1 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
  • 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
  • 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·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·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 J4500E, D45CRTELE, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide