Device recall
Z-0150-2015: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are…
FDA device recall · Class II · Medartis, Inc.
Key facts
| Recall number (Z-number) | Z-0150-2015 |
|---|---|
| Recall event | 69433 |
| Product | APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna. |
| Product code | HWC |
| Recalling firm | Medartis, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2015 |
| 510(k) numbers | K141232 |
| FEI number | 3005215824 |
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