Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3207-2024 — Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve

U.S. FDA — Device Enforcement · United States · 2024-08-21 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3207-2024
Date of alert
2024-08-21
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Percussionaire Corporation
Product category
device
Product type
Devices
Reported risk: Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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