Device recall
Z-2617-2026: Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below…
FDA device recall · Class II · DEPUY (IRELAND)
Key facts
| Recall number (Z-number) | Z-2617-2026 |
|---|---|
| Recall event | 99078 |
| Product | Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 10mm B; Part Number: 151730410. 2. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 12mm B; Part Number: 151730412. 3. ATTUNE KNEE SYSTEM… |
| Product code | KRO |
| Recalling firm | DEPUY (IRELAND) |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K242871 |
| FEI number | 3002854251 |
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