Device recall
Z-0838-2018: ACL DISPOSABLE PACK BONE-TENDON-BONE, Model 0234020280, labeled sterile.
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0838-2018 |
|---|---|
| Recall event | 78668 |
| Product | ACL DISPOSABLE PACK BONE-TENDON-BONE, Model 0234020280, labeled sterile. |
| Product code | KDD |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2024 |
| FEI number | 2936485 |
At a glance
- None 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