Recall Z-3221-2026— Ventec Life Systems, Inc.
Class II · Ongoing
Class II FDA medical device recall by Ventec Life Systems, Inc., initiated 2026-07-28. FDA's recall record names no specific 510(k) clearance for this event. Product: HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve. Reason: Labeling; Oxygen Cylinders do not contain required medical gas labeling.
- Recalling firm
- Ventec Life Systems, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-28
- Firm location
- Bothell, WA, United States
Product description
HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
Reason for recall
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Data sourced from openFDA. This site is unofficial and independent of the FDA.