Device recall
Z-1218-2025: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate…
FDA device recall · Class II · Tyber Medical
Key facts
| Recall number (Z-number) | Z-1218-2025 |
|---|---|
| Recall event | 96212 |
| Product | A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708122 Product Description: |
| 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