Has Percussionaire Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 7 total FDA actions tied to Percussionaire Corporation: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-10-07; Argus observed and indexed it on 2026-10-13.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with I…

Name: FDA Recall Record — Percussionaire Corporation
Creator: Argus HQ
Published: 2026-10-07
License: https://argushq.ai/methodology

Event date: 2026-10-07 00:00:00Z
Observed: 2026-10-13 04:20:34Z
Source ID: Z-3323-2026
Payload hash: 29a7e68ac77438ae5cc73e64…

Summary

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, ta… Status: Ongoing.

Entities

Percussionaire Corporation

View source record ↗

Frequently asked questions

Has Percussionaire Corporation had other FDA enforcement actions?: Yes. Argus HQ has recorded 7 total FDA actions tied to Percussionaire Corporation: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-10-07; Argus observed and indexed it on 2026-10-13.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010,  Phasitron 5, Product Number: P5 used with I…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-percussionaire-corporation-z-3323-2026

MLA

"Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010,  Phasitron 5, Product Number: P5 used with I…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-percussionaire-corporation-z-3323-2026.

Chicago

Argus HQ Research. "Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010,  Phasitron 5, Product Number: P5 used with I…." Digital Empire Holdings LLC. Accessed October 13, 2026. https://argushq.ai/events/fda-recall-percussionaire-corporation-z-3323-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_percussionaire_corporation_z_3323_2026_2026,
  title = {Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010,  Phasitron 5, Product Number: P5 used with I…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-percussionaire-corporation-z-3323-2026},
  note = {Accessed: October 13, 2026}
}

Informational only. Not legal, financial, or medical advice.