Device recall
Z-1601-2026: I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions…
FDA device recall · Class II · I.T.S. GmbH
Key facts
| Recall number (Z-number) | Z-1601-2026 |
|---|---|
| Recall event | 98341 |
| Product | I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1. Distal Tubular Plate; Article Numbers: 21602-3, 21602-4, 21602-5, 21602-6, 21602-7, 21602-8, 21603-3, 21603-4, 21603-5, 21603-6, 21603-7, 21603-8. 2. Fibula Plate 3.5mm; Article… |
| Product code | HRS |
| Recalling firm | I.T.S. GmbH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K063672 |
| FEI number | 3004369035 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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