Device recall
Z-1983-2008: Margron DTC Hip Replacement System; Margron hip - Femoral stem + suture holes…
FDA device recall · Class II · Portland Orthopaedics Pty, Ltd.
Key facts
| Recall number (Z-number) | Z-1983-2008 |
|---|---|
| Recall event | 47369 |
| Product | Margron DTC Hip Replacement System; Margron hip - Femoral stem + suture holes 4+4, sterile, Portland Orthopaedics Inc., St. Clair, MI; REF 2-662-944. Product is used for Orthopedic surgery. Product is used for Orthopedic surgery. |
| Product code | MEH |
| Recalling firm | Portland Orthopaedics Pty, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2009 |
| 510(k) numbers | K032641, K992815 |
| FEI number | 3003755751 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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