# FDA recall Z-3223-2026

> **Ventec Life Systems, Inc.** · Class II · device recall initiated 2026-07-28.

## Product

REF: HF2POSTD  HomeFill Oxygen System  HomeFill cylinder D with CGA870 Compatible Post Valve

## Reason for recall

Labeling; Oxygen Cylinders do not contain required medical gas labeling

## Distribution

US Nationwide distribution in the states of FL, IA, OH, NE, TN.

## Key facts

- **Recall number:** Z-3223-2026
- **Recalling firm:** Ventec Life Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-28
- **Report date:** 2026-09-30

- **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-3223-2026

## Citation

> MORVS. FDA recall Z-3223-2026. Retrieved 2026-10-22 from https://api.morvs.ai/recall/Z-3223-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*