Percussionaire Corporation recalls
Every recall we track for Percussionaire Corporation — 15 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Percussionaire Corporation fell by more than half in 2025 (1, down from 4 in 2024). 7% rated “stop using now”.
All FDA recall records for Percussionaire Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 1 | 0 | 1 | 0 | 2 |
| 2024 | 0 | 1 | 3 | 0 | 4 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 1 | 0 | 6 | 7 |
What to do if you have a recalled Percussionaire Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Percussionaire Corporation recalls
8 shown- Use cautionMedical device
Percussionaire Corporation recalls Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC
Percussionaire Corporation recalls Intrapulmonary Percussive Ventilation (IPV) HC due to risk of altered anesthetic delivery causing hypertonia, hypotonia, tachycardia, bradycardia, elevated intracranial pressure, or awareness during anesthesia.
Percussionaire CorporationAug 18, 2026 - Use cautionMedical device
Percussionaire Corporation recalls Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE
Percussionaire recalls Phasitron 5 In-Line Valves (P5-TEE-20/P5-TEE) that may leak when used with ventilators, risking respiratory failure in neonates or infants under 10kg with low tidal volumes.
PercussionaireSep 17, 2025 - Use cautionMedical device
Percussionaire Corporation recalls VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single
Percussionaire recalls VDR4 Phasitron Breathing Circuits with venturi component that may cause reduced ventilation. Affected models include specific kits and units with listed lot codes.
PercussionaireDec 23, 2024 - Lower riskMedical device
Percussionaire Corporation recalls Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to
Percussionaire recalls Phasitron5 Breathing Circuits (P5-10, P5-HC, P5-UC-10) due to discolored fluid from nickel coating reactions with medication. Affected units sold with specific lot numbers.
PercussionaireSep 16, 2024 - Lower riskMedical device
Percussionaire Corporation recalls Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line
Percussion: Percussionaire recalls 20 IPV therapy in-line valves with specific serial numbers due to updated labeling requirements for blue cap removal before use.
PercussionaireAug 21, 2024 - Stop using nowMedical device
Percussionaire Corporation recalls High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
Percussionaire recalls High Frequency Transport Phasitron Breathing Circuit Kit REF A50605-D (Rx Only) due to assembly errors causing potential severe pressure output issues. Affected units have specific lot numbers and were sold with CE 0123 marking.
PercussionaireDec 12, 2023 - Lower riskMedical device
Percussionaire Corporation recalls Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Percussionaire recalls Distal Phasitron Part S20020 for use with VDR-4 control units due to potential assembly error causing less effective therapy. Affected units have specific UDI-DI and expiration dates.
PercussionaireMar 28, 2023 - Lower riskMedical device
Percussionaire Corporation recalls Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators.
Percussionaire recalls Monitron II Waveform Analyzers (REF S00015-1) used with ventilators due to screen freezes that may cause display issues during critical medical monitoring.
PercussionaireSep 14, 2020
Percussionaire Corporation recall questions
How many recalls has Percussionaire Corporation had?
15 recalls from Percussionaire Corporation are on record with U.S. safety agencies, from 2020–2026.
What is the most recent Percussionaire Corporation recall?
Percussionaire Corporation recalls Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC, dated Aug 18, 2026. Every Percussionaire Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Percussionaire Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Percussionaire Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.