Device recall
Z-1419-2022: ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation…
FDA device recall · Class II · DePuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1419-2022 |
|---|---|
| Recall event | 90557 |
| Product | ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525 |
| Product code | HWT |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1818910 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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