Device recall
Z-3109-2011: REF 91200, Juggerknot system, Soft Anchors, -Two implants size 1, Biomet Sports…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-3109-2011 |
|---|---|
| Recall event | 59366 |
| Product | REF 91200, Juggerknot system, Soft Anchors, -Two implants size 1, Biomet Sports Medicine, STERILE. Product Usage: The JuggerKnot Soft Anchors include various size ranges, each consisting of a coreless sleeve and suture(s) assembled on an inserter instrument. The system includes instrumentation… |
| Product code | MBI |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2013 |
| 510(k) numbers | K110145 |
| 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