# FDA recall Z-1196-2025

> **Ventec Life Systems, Inc.** · Class I · device recall initiated 2025-02-03.

## Product

VOCSN Multi-Function Ventilators:  VOCSN+Pro (V+O+C+S+N+Pro, English), REF:  PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000, PRT-01185-002

## Reason for recall

Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on patient efforts, less inspiratory volume, less inspiratory pressure, and less PEEP delivered.

## Distribution

US distribution in CA, NY, and MO.

## Key facts

- **Recall number:** Z-1196-2025
- **Recalling firm:** Ventec Life Systems, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-03
- **Report date:** 2025-03-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bothell, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1196-2025

## Citation

> AI Analytics. FDA recall Z-1196-2025. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1196-2025. Source: US FDA. Licensed CC0.

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