Device recall
Z-1820-2013: LPS Lower Extremity Dovetail Intercalary component. Intended for use in…
FDA device recall · Class I · DePuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1820-2013 |
|---|---|
| Recall event | 65591 |
| Product | LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-shaft portion of the femur. |
| Product code | JWH |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 10, 2014 |
| 510(k) numbers | K041085 |
| FEI number | 1818910 |
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