Device recall
Z-0366-2020: TriMed Olecranon Hook Plate, Lt, 6-Holes, REF: OHOOKL-6, Non-Sterile, RX only…
FDA device recall · Class II · TriMed Inc.
Key facts
| Recall number (Z-number) | Z-0366-2020 |
|---|---|
| Recall event | 83984 |
| Product | TriMed Olecranon Hook Plate, Lt, 6-Holes, REF: OHOOKL-6, Non-Sterile, RX only, (01) 00842188101281 - Product Usage: The OHOOKL is a semi-tubular design bone plate with two offset intramedullary tines, which are intended to penetrate the small terminal fragment to provide additional stabilization. |
| Product code | HRS |
| Recalling firm | TriMed Inc. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K060041 |
| 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