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Percussionaire Corporation recalls Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Val
Recalled October 9, 2024 · FDA recall Z-3208-2024 · Percussionaire
Hazard
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy. · FDA Class I
Units
2523 units
Sold at
US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey
Description
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
Product
Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve
Manufacturer(s)
Percussionaire Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →