Percussionaire Corporation: Medical Device Recall in 2024 - (Recall #: Z-3207-2024)

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, Qty: 1, 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-3207-2024

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: 50,460 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