Device recall
Z-1673-2015: LCS COMPLETE RPS inserts, various sizes. Knee prosthesis component for…
FDA device recall · Class II · DePuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1673-2015 |
|---|---|
| Recall event | 71085 |
| Product | LCS COMPLETE RPS inserts, various sizes. Knee prosthesis component for orthopedic surgery. |
| Product code | NJL |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 30, 2015 |
| PMA numbers | P830055 |
| FEI number | 1818910 |
At a glance
- None 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