Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Val
- Recalling company
- Ventec Life Systems, Inc.
- Product
- REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D 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
- 25 units
- Lot / codes
- UDI:00850018761376/ Serial #s: 25EKMA00BAC 25EKMA009L3 25EKMA009CM 25EKMA009J8 25GKMA00077 25GKMA0007B 25GKMA0009Z 25GKMA0004U 25GKMA000CS 25GKMA000CR 25GKMA000CX 25GKMA000D0 25GKMA000LL 25GKMA000N1 25GKMA000UD 25GKMA000D1 25GKMA000TN 25GKMA000D2 25GKMA000UC 25GKMA000LK 25GKMA000UA 25GKMA000UB 25GKMA000UE 25GKMA000CY 25GKMA000UF
- Company location
- Bothell, WA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3223-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3223-2026 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.