Percussionaire Corporation: Medical Device Recall in 2024 - (Recall #: Z-0693-2024)

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:

Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)

Product Classification:

Class I

Date Initiated: March 28, 2023

Date Posted: January 24, 2024

Recall Number: Z-0693-2024

Event ID: 93648

Reason for Recall:

Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.

Status: Ongoing

Product Quantity: 195

Code Information:

UDI-DI: 00849436000693, Lots/Expiration: WO03739/September 13, 2024, and WO04218/November 14, 2024.

Distribution Pattern:

US: RI, CA, TX

Voluntary or Mandated:

Voluntary: Firm initiated