Recall Z-0031-2026— Percussionaire Corporation
Class I · Ongoing
Class I FDA medical device recall by Percussionaire Corporation, initiated 2025-09-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use. Reason: IFU update; in-line valve, with pressure relief seal may leak when used with ventilator; don't use in neonates/infants, with target tidal volumes less-than50mL or less-than10kg- at high risk of cardiopulmonary/neurological compromise due to unrecognized hypoventilation, updates for continued use in others before design update; leak may cause respiratory acidosis, hypoxemia, or respiratory failure..
- Recalling firm
- Percussionaire Corporation
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2025-09-17
- Firm location
- Sandpoint, ID, United States
Product description
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use
Reason for recall
IFU update; in-line valve, with pressure relief seal may leak when used with ventilator; don't use in neonates/infants, with target tidal volumes less-than50mL or less-than10kg- at high risk of cardiopulmonary/neurological compromise due to unrecognized hypoventilation, updates for continued use in others before design update; leak may cause respiratory acidosis, hypoxemia, or respiratory failure.
Data sourced from openFDA. This site is unofficial and independent of the FDA.