Ventec Life Systems, Inc. recalls HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- Recalling company
- Ventec Life Systems, Inc.
- Product
- HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- Reason
- Labeling; Oxygen Cylinders do not contain required medical gas labeling
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 28, 2026
- Reported
- Sep 30, 2026
- Distribution
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- Status
- Ongoing
- Quantity
- 21 units
- Lot / codes
- UDI:00850018761369/Serial #s: 24IKMA00532 24IKMA0053M 24IKMA0054N 24IKMA005G8 24IKMA005AP 24IKMA005QB 24IKMA005Q4 24IKMA005PM 24IKMA005QJ 24IKMA005QX 24IKMA005PJ 24IKMA005SW 24IKMA005RB 24IKMA00612 24IKMA0067E 24IKMA0066L 24IKMA0068U 24IKMA00685 24IKMA006AQ 24IKMA006B7 24IKMA006BG
- Company location
- Bothell, WA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3221-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3221-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.