Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Distal Phasitron Recalled by Percussionaire Corporation Due to Breathing circuit reservoir bag may be assembled at...

Date: March 28, 2023
Company: Percussionaire Corporation
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Percussionaire Corporation directly.

Affected Products

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

Quantity: 195

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 3 states: CA, RI, TX

Affected (3 states)Not affected

About Percussionaire Corporation

Percussionaire Corporation has 8 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report