Class II — Ventec Life Systems, Inc.
| Recalling firm | Ventec Life Systems, Inc. |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | Labeling; Oxygen Cylinders do not contain required medical gas labeling |
| Product | HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve |
| Quantity | 21 units |
| Distribution | US Nationwide distribution in the states of FL, IA, OH, NE, TN. |
| Initiated | 2026-07-28 |
| Classified | 2026-09-18 |
| Recall number | Z-3221-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Ventec Life Systems, Inc. (Z-3221-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99660/
Alerts for Ventec Life Systems, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.