Class I

Medical Device Recall: Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve

Percussionaire Corporation · August 21, 2024

Reason for Recall

Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.

Distribution

US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey

States Affected

NATIONWIDE

Quantity Affected

2523 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3208-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Percussionaire Corporation Medical Device Recall: Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve | SafeCheck