FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled July 1, 2026

VOCSN+Pro package recall — Ventec Life Systems, Inc.

Hazard: Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2525-2026
Brand
Ventec Life Systems
Classification
Class II
Units affected
1
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001

Affected products

Companies & origin

Recalling firm location
Bothell, WA, United States
Firm address
22002 26th Ave Se, N/A, 98021-4903

Identifying details (verbatim from the notice)

Product codes / lots
REF/UDI-DI/Serial Number/Lot: PRT-00853-000/00855573007839/155391P/807138, PRT-00490-001/00855573007792/155391/804613
Distribution
US Nationwide distribution in the state of UT.
Firm notified the public via
Letter
FDA event ID
98888
Recall initiated
May 8, 2026
FDA classified
June 23, 2026
FDA report date
July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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