Device recall
Z-1132-2026: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist…
FDA device recall · Class II · Tyber Medical
Key facts
| Recall number (Z-number) | Z-1132-2026 |
|---|---|
| Recall event | 98214 |
| Product | Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No |
| 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
- 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