Ventec Life Systems, Inc. recalls REF:HF2PC9 HomeFill Oxygen System
- Recalling company
- Ventec Life Systems, Inc.
- Product
- REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver
- 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
- 2 units
- Lot / codes
- UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM
- Company location
- Bothell, WA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3222-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3222-2026 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.