Official recall record
Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number:
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-08-18
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00849436000679
- Brand on record
- Percussionaire Corporation
What the authority reported
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, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-23.
Record last checked against the registry on 2026-10-23.
Other recalls from this brand
- 2026-08-18 · US FDA — Medical Devices
In-Line Valve, Product Number: P5-TEE - 2026-08-18 · US FDA — Medical Devices
Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC - 2026-08-18 · US FDA — Medical Devices
Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
All 9 official recall notices naming Percussionaire Corporation on this site →
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