Percussionaire Corporation: Medical Device Recall in 2024 - (Recall #: Z-3208-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: August 21, 2024

Date Posted: October 9, 2024

Recall Number: Z-3208-2024

Event ID: 95239

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.

Status: Ongoing

Product Quantity: 2523 units

Code Information:

No UDI/Lots: 240620 240610 240418 240326 230612 WO07066 WO07010 WO06020 WO05019 WO04884 WO04827 WO04756 WO04714 WO04656 WO04625 WO04596 WO04553 WO04398 WO04356 WO04061 WO03846 WO03748 WO03688

Distribution Pattern:

US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey

Voluntary or Mandated:

Voluntary: Firm initiated