FDA recall Z-3223-2026

Ventec Life Systems, Inc. · Class II · device

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

Status
Ongoing
Initiation date
2026-07-28
Report date
2026-09-30
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bothell, WA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3223-2026