REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post... recall (Ventec Life Systems, Inc.)
Medical deviceClass IIOngoing
Summary: Ventec Life Systems, Inc. is recalling REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve. Reason: Labeling; Oxygen Cylinders do not contain required medical gas labeling.
What is being recalled
REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Why
Labeling; Oxygen Cylinders do not contain required medical gas labeling
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of FL, IA, OH, NE, TN. (states named: Florida, Iowa, Nebraska, Ohio, Tennessee)
How to tell if yours is affected
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
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-3223-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | July 28, 2026 |
| Reported | September 30, 2026 |
| Company | Ventec Life Systems, Inc. |
| Company location | Bothell, WA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 25 units |
More recalls from Ventec Life Systems, Inc. · all medical device recalls · recalls from July 2026