Device recall
Z-1902-2021: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog…
FDA device recall · Class II · Ventec Life Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1902-2021 |
|---|---|
| Recall event | 87838 |
| Product | Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog Number: V+O+C+S+N+Pro/English/PRT-00490-001; V+O+C+S+N+Pro/Japan/PRT-00490-100; V+C+Pro/English/PRT-00900-001; V+C+Pro/Japan/PRT-00900-100; V+C/English/PRT-01098-000; V+O+C+S+N/English/PRT-01100-000… |
| Product code | CBK |
| Recalling firm | Ventec Life Systems, Inc. |
| Recall class | Class II |
| 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
- 100–999 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