Fresh Recalls

Ventec Life Systems recalls

5 recent recalls on record for Ventec Life Systems in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve (1)REF (2)VOCSN V+Pro package (1)VOCSN+Pro package (1)

All Ventec Life Systems recalls

FDA Class II · Medical device · September 30, 2026

REF recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Official ID Z-3223-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

REF recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Official ID Z-3222-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Official ID Z-3221-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

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

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 back…

Official ID Z-2525-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

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

Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing…

Official ID Z-1942-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.