Device recall
Z-1448-2014: Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid…
FDA device recall · Class II · Pega Medical Inc.
Key facts
| Recall number (Z-number) | Z-1448-2014 |
|---|---|
| Recall event | 67675 |
| Product | Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft), Part number: M040-SS-110; Used in Implant Catalogue number: FD-040(LS)-SS. orthopedic intramedullary rod. |
| Product code | HSB |
| Recalling firm | Pega Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2014 |
| 510(k) numbers | K020885, K041393 |
| FEI number | 3000327445 |
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