The Recall Desk

Hazard

Technical Distortion recalls

3 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2023-12-06

Of the 3 technical distortion recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all technical distortion recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–3 of 3

  • HighFDA (Devices)·Z-0404-2024·2023-12-06

    Medical Device Recall: SENTIERO Hearing Screening Devices for Technical Distortions

    PATH's SENTIERO SCREENING hearing examination devices (Model SOH100098) are being recalled due to technical distortions that may exceed expected levels. The recall affects devices distributed in Florida, Missouri, Ohio, and Wisconsin.

    Product
    SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0401-2024·2023-12-06

    SENTIERO Hearing Examination Device Recalled for Technical Distortions

    PATH recalls SENTIERO hearing examination devices for excessive technical distortions. Affected units are distributed in FL, MO, OH, and WI.

    Product
    SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0403-2024·2023-12-06

    Medical device for hearing exams recalled for technical distortion issues

    PATH is recalling AuDX PRO hearing examination devices because they may produce technical distortions greater than expected, which could affect diagnostic accuracy. The recall affects 23 units distributed in Florida, Missouri, Ohio, and Wisconsin.

    Product
    AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
    Category
    Medical Device
    Distribution
    4 states