Device recall
Z-0582-2012: Artificial Ligament Fixation Device 15MM TI NS ToggleLoc (TM) W/Continuous…
FDA device recall · Class II · Biomet Sports Medicine
Key facts
| Recall number (Z-number) | Z-0582-2012 |
|---|---|
| Recall event | 48745 |
| Product | Artificial Ligament Fixation Device 15MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament Fixation Device 25MM TI NS ToggleLoc (TM) W/Continuous Maxbraid Polyethylene Suture Loop TO Gal 4V Alloy/Polyethylene; Artificial Ligament… |
| Product code | MBI |
| Recalling firm | Biomet Sports Medicine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 27, 2011 |
| 510(k) numbers | K033838 |
| 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