Device recall
Z-1942-2026: VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
FDA device recall · Class I · Ventec Life Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1942-2026 |
|---|---|
| Recall event | 98554 |
| Product | VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000 |
| Product code | NOU |
| Recalling firm | Ventec Life Systems, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K162877 |
| FEI number | 3013095415 |
At a glance
- 1–9 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