The Recall Desk

Hazard

Respiratory Irritation recalls

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

What the numbers show

Total
4
Critical
0
Severe
1
Most recent
2025-03-27

Of the 4 respiratory irritation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (25%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all respiratory irritation 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.

1–4 of 4

  • HighCPSC·25197·2025-03-27

    Cra-Z-Art Gemex and Gel2Gem Jewelry Kits Recalled for Chemical Irritation Risk

    LaRose Industries is recalling about 224,100 Cra-Z-Art Gemex and Gel2Gem jewelry kits because the resin liquid can cause skin, eye, and respiratory irritation in children when inhaled, touched, or ingested.

    Product
    Cra-Z-Art Gemex/Gel2Gem Jewelry Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1074-2025·2025-02-19

    Sevoflurane Vaporizer Quik-Fil Recalled Due to Chemical Degradation Risk

    A sevoflurane vaporizer component may degrade to hydrogen fluoride, causing respiratory damage and chemical burns to patients and workers. FDA classified this Class I recall affecting six units in Kentucky and Connecticut.

    Product
    Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.
    Category
    Medical Device
    Distribution
    2 states
  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide