Device recall
Z-1226-2025: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right…
FDA device recall · Class II · Tyber Medical
Key facts
| Recall number (Z-number) | Z-1226-2025 |
|---|---|
| Recall event | 96212 |
| Product | A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715162 |
| Product code | HRS |
| Recalling firm | Tyber Medical |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K232652 |
| FEI number | 3012966183 |
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