The Recall Desk

Hazard

Incorrect Report recalls

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

What the numbers show

Total
2
Critical
0
Severe
0
Most recent
2019-12-04

Of the 2 incorrect report 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 incorrect report 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.

1–2 of 2

  • HighFDA (Devices)·Z-0547-2020·2019-12-04

    V-Twin In Vitro Diagnostic Instruments Recalled for Sample Mismatch Risk

    Vital Scientific N.V. is recalling 732 V-Twin instruments in New York due to a risk of aspirating samples from the wrong container, which could lead to incorrect patient reports.

    Product
    V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0283-2016·2015-11-25

    Agfa Healthcare Recalls IMPAX CV Software for Incorrect PDF Reports

    Agfa Healthcare is recalling IMPAX CV software versions 7.8.x and 12.x because the Demographics Manager feature may generate incorrect PDF reports after physician signature.

    Product
    IMPAX, PACS, Picture Archive and Communications System, IMPAX CV 7.8.x and IMPAX CV 12.x. Corrects certain demographic information (Patient Name, Patient Medical Record Number and/or Accession Number in previously signed reports that have since changed.
    Category
    Medical Device
    Distribution
    13 states