The Recall Desk

Hazard

Inhalation recalls

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

What the numbers show

Total
7
Critical
0
Severe
1
Most recent
2026-06-17

Of the 7 inhalation 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 (14%) 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 inhalation 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.

1–7 of 7

  • HighFDA (Drugs)·D-0607-2026·2026-06-17

    Budesonide inhalation ampules contain black and brown specks and particles

    Budesonide Inhalation Suspension, 1 mg/2 mL single-dose ampules from Sun Pharmaceutical, is being recalled after a quality complaint of black or brown specs and particles in the solution.

    Product
    BUDESONIDE — BUDESONIDE (BUDESONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1613-2023·2023-05-31

    Olympus Single Use Distal Cover for Endoscope Recalled Due to Detachment Risk

    Olympus is recalling about 309,278 single-use endoscope covers that may detach during use, risking aspiration, inhalation, obstruction, or burns.

    Product
    Olympus Single Use Distal Cover Model Number MAJ-2315 used with EVIS EXERA III Duodenovideoscope TJF-Q190V; Item code: Catalogue #N5786100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1956-2021·2021-07-21

    Philips Respironics Continuous Ventilators Recalled for Foam Degradation Risk

    Philips Respironics is recalling approximately 255,810 continuous ventilators because polyurethane foam may degrade into particles that could be inhaled or ingested, or release chemicals.

    Product
    Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·96188·1996-09-11

    Gerber Recalls Flip Fingers Rattles Due to Choking Hazard

    Gerber is recalling approximately 60,000 Flip Fingers Rattles because spherical end-caps may separate, releasing small parts that pose a choking and inhalation hazard to young children.

    Product
    Gerber Flip Fingers Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·95110·1995-04-26

    Philip Morris Recalls Parliament Key Chains Containing Liquid Petroleum

    Philip Morris is recalling approximately 500,000 Parliament key chains distributed in the northeastern U.S. and Florida because they contain liquid petroleum that poses a hazard to young children.

    Product
    CPSC, Philip Morris And Cyrk Announce Recall Of Key Chains
    Category
    Consumer Product
    Distribution
    Distributed nationwide