Device recall
Z-1705-2013: REF 154214 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C3…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1705-2013 |
|---|---|
| Recall event | 65459 |
| Product | REF 154214 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing tibial component for use in… |
| Product code | HRY |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2014 |
| 510(k) numbers | K122277 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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