Device recall
Z-0020-2019: CAPNOSTREAM 20 (US) N, Part Number CS08651
FDA device recall · Class II · Oridion Medical 1987 Ltd.
Key facts
| Recall number (Z-number) | Z-0020-2019 |
|---|---|
| Recall event | 80895 |
| Product | CAPNOSTREAM 20 (US) N, Part Number CS08651 |
| Product code | DQA |
| Recalling firm | Oridion Medical 1987 Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 20, 2022 |
| 510(k) numbers | K082268 |
| FEI number | 3001227743 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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