Device recall
Z-1478-2012: REF 28234 Troch Nail, Long 11MM, Right 34 CM Peritrochanteric Nail System, Rx…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1478-2012 |
|---|---|
| Recall event | 61658 |
| Product | REF 28234 Troch Nail, Long 11MM, Right 34 CM Peritrochanteric Nail System, Rx Sterile Biomet Trauma Persippany, NJ Rod, Fixation, Intramedullary and Accessories Product Usage: An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as… |
| Product code | HSB |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2013 |
| 510(k) numbers | K050118 |
| FEI number | 1825034 |
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