Device recall
Z-0560-2010: Toggleloc System, Biomet Ziptight Ankle Syndesmosis Fixation System - SS with…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0560-2010 |
|---|---|
| Recall event | 53878 |
| Product | Toggleloc System, Biomet Ziptight Ankle Syndesmosis Fixation System - SS with Ziploop Technology, polyethylene/polypropylene/ polyester/ stainless steel, sterile Biomet Sports Medicine, Warsaw, IN.; REF 909857. A smooth or threaded metallic bone fixation fastener intended to be implanted for… |
| Product code | MBI |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2010 |
| 510(k) numbers | K083070 |
| 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