Skip to main content
Recall Canary
VOCSN V+Pro Respiratory System
← Back to all recalls
MEDICAL DEVICE RECALLCRITICAL

VOCSN V+Pro Respiratory System

Ventec is recalling VOCSN V+Pro respiratory systems (REF: PRT-01198-000, PRT-01185-000) due to potential oxygen leaks that may increase fire risk.

What to do

Stop using the VOCSN V+Pro respiratory system immediately and contact Ventec Life Systems for instructions on replacement or repair. Do not operate the device until you receive guidance from the manufacturer.

Recalled
Listed
Updated
Recall No.
Z-1942-2026
Agency
FDA
Firm
Ventec Life Systems, Inc.
Recall ID
98554
Status
ONGOING

Why it was recalled

Ventec Life Systems is recalling VOCSN V+Pro respiratory systems (REF: PRT-01198-000 package; REF: PRT-01185-000 unit) because they may not have been fully evaluated under high-pressure conditions during production testing. An oxygen leak could occur, resulting in reduced oxygen delivery and creating an oxygen-enriched environment that increases fire risk.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000

UDI-DI
00855573007914, 00855573007877

Where it was sold

Distributed in California, Georgia, Missouri, and Ohio.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other recent recalls from Ventec Life Systems, Inc.

All recalls from Ventec Life Systems, Inc.

← Back to all recalls

Editorial summary by Recall Canary · summary updated 2026-05-02 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification