Device recall
Z-1782-2008: BIOMET EZLoc 7-8mm TM Femoral Fixation, Catalog Number 904780. The Ezloc Is…
FDA device recall · Class II · Biomet Sports Medicine
Key facts
| Recall number (Z-number) | Z-1782-2008 |
|---|---|
| Recall event | 47859 |
| Product | BIOMET EZLoc 7-8mm TM Femoral Fixation, Catalog Number 904780. The Ezloc Is indicated for use for fixation of tendons & ligaments during orthopedic reconstruction procedures such as Anterior Cruciate Ligament (ACL) reconstruction. |
| Product code | MBI |
| Recalling firm | Biomet Sports Medicine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2012 |
| 510(k) numbers | K041261 |
| FEI number | 1000125597 |
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