Device recall
Z-3222-2026: REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated…
FDA device recall · Class II · Ventec Life Systems, Inc.
Key facts
| Recall number (Z-number) | Z-3222-2026 |
|---|---|
| Recall event | 99660 |
| Product | REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver |
| Product code | ECX |
| Recalling firm | Ventec Life Systems, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013095415 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database