Device recall
Z-1569-2025: restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number…
FDA device recall · Class II · Conformis Inc.
Key facts
| Recall number (Z-number) | Z-1569-2025 |
|---|---|
| Recall event | 96606 |
| Product | restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip System |
| Product code | LPH |
| Recalling firm | Conformis Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K202484 |
| FEI number | 3004153240 |
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