Device recall
Z-2698-2011: Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE…
FDA device recall · Class II · Biomet U.K., Ltd.
Key facts
| Recall number (Z-number) | Z-2698-2011 |
|---|---|
| Recall event | 58702 |
| Product | Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UNLESS PACK DAMAGED, BIOMET UK Ltd, (510K# K011138) This device is used in partial knee replacement surgery as a result of patients who are experiencing degenerative arthritis. |
| Product code | HRY |
| Recalling firm | Biomet U.K., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 3, 2011 |
| 510(k) numbers | K011138 |
| FEI number | 3002806535 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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