Device recall
Z-2057-2018: 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2057-2018 |
|---|---|
| Recall event | 79978 |
| Product | 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints. |
| Product code | PPR |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Completed |
| FEI number | 2936485 |
At a glance
- None 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