Device recall
Z-0943-03: Fixion PF (''Proximal Femur'') Hip Peg. Fixion PF Hip Pegs are manufactured in…
FDA device recall · Class III · Disc Orthopaedic Technologies Inc
Key facts
| Recall number (Z-number) | Z-0943-03 |
|---|---|
| Recall event | 25800 |
| Product | Fixion PF (''Proximal Femur'') Hip Peg. Fixion PF Hip Pegs are manufactured in the following various lengths; 80mm, 81mm, 90mm, 91mm, 100mm, 101mm, 105mm, 110mm, 111mm, 120mm, and 121mm. The Fixion PF Hip Peg is intended for use in the fixation of proximal fractures in the femur. |
| Product code | NDH |
| Recalling firm | Disc Orthopaedic Technologies Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 8, 2003 |
| 510(k) numbers | K010988, K012967, K021324 |
| FEI number | 3003363248 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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