Class II

Medical Device Recall: HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve

Ventec Life Systems, Inc. · July 28, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

21 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3221-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Ventec Life Systems, Inc. Medical Device Recall: HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve | SafeCheck