Percussionaire Corporation — FDA Compliance Timeline

FDA action counts

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Percussionaire Corporation has 7 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Enforcement history

On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron…. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV-2C, Product Number: S00002-C; Phasit…. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with In…. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron…. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: In-Line Valve, Product Number: P5-TEE. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasit…. On 2026-10-07, Argus HQ recorded an FDA recall for Percussionaire Corporation, rated "high" severity in Argus HQ's classification: Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with I…. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Frequently asked questions

Has Percussionaire Corporation had product recalls?

Yes, 7 recalls on file. See the full history below for each one.

Is this FDA enforcement data for Percussionaire Corporation official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has Percussionaire Corporation had?

Argus HQ has recorded 7 FDA events for Percussionaire Corporation: 0 warning letters, 7 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against Percussionaire Corporation?

The most recent FDA event Argus HQ has on file for Percussionaire Corporation is dated 2026-10-07, with a severity rating of "high" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Related enforcement actions

• Percussionaire Corporation — Class II recall: Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with I… →
• Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasit… →
• Percussionaire Corporation — Class II recall: In-Line Valve, Product Number: P5-TEE →
• Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron… →
• Percussionaire Corporation — Class II recall: Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with In… →
• Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV-2C, Product Number: S00002-C; Phasit… →
• Percussionaire Corporation — Class II recall: Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron… →

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