Device recall
Z-2224-2012: Oxford Gap Gauge SML 3/4mm. The instrument is used for an intermediate check of…
FDA device recall · Class II · Biomet U.K., Ltd.
Key facts
| Recall number (Z-number) | Z-2224-2012 |
|---|---|
| Recall event | 62745 |
| Product | Oxford Gap Gauge SML 3/4mm. The instrument is used for an intermediate check of the flexion and extension gaps when preparing the femur to accept the femoral component. |
| Product code | IQO |
| Recalling firm | Biomet U.K., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 15, 2013 |
| FEI number | 3002806535 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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