Percussionaire Corporation: Medical Device Recall in 2024 - (Recall #: Z-0637-2024)

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:

High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123

Product Classification:

Class I

Date Initiated: December 12, 2023

Date Posted: January 24, 2024

Recall Number: Z-0637-2024

Event ID: 93476

Reason for Recall:

Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user

Status: Ongoing

Product Quantity: 2145 units

Code Information:

UDI: (01)10849436000331/Lot # WO05216, WO05254, WO05321, WO05392, WO05559, WO05588, WO05684, WO05749, WO05896, WO05930,WO06028

Distribution Pattern:

US:AL AR CA CT FL GA IL IN KS LA MI MN MO NC NJ OH OR TN TX UT VA OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated