Device recall
Z-0831-2013: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with…
FDA device recall · Class I · DePuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-0831-2013 |
|---|---|
| Recall event | 63783 |
| Product | LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bony defects. |
| Product code | MBH |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 20, 2014 |
| 510(k) numbers | K071417 |
| 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