Device recall
Z-0191-2010: Biomet 5.5 mm peek Allthread PEEK Knotless Anchor, knotless, sterile, Biomet…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0191-2010 |
|---|---|
| Recall event | 53581 |
| Product | Biomet 5.5 mm peek Allthread PEEK Knotless Anchor, knotless, sterile, Biomet sports Medicine, Inc., Ontario, CA; REF 904842P. Intended to be implanted for fixation of bone fractures and for bone reconstructions. |
| Product code | HWC |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2011 |
| 510(k) numbers | K070389 |
| 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