Device recall
Z-2877-2018: Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S…
FDA device recall · Class II · TriMed Inc.
Key facts
| Recall number (Z-number) | Z-2877-2018 |
|---|---|
| Recall event | 80487 |
| Product | Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna. |
| Product code | HRS |
| Recalling firm | TriMed Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2021 |
| 510(k) numbers | K043263 |
| FEI number | 3001236812 |
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