Device recall
Z-2931-2018: N Latex CDT Kit
FDA device recall · Class II · CSL Behring GmbH
Key facts
| Recall number (Z-number) | Z-2931-2018 |
|---|---|
| Recall event | 80431 |
| Product | N Latex CDT Kit |
| Product code | NAO |
| Recalling firm | CSL Behring GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2021 |
| 510(k) numbers | K060677 |
| FEI number | 3003098680 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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