Device recall
Z-1124-2013: REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF…
FDA device recall · Class II · Biomet U.K., Ltd.
Key facts
| Recall number (Z-number) | Z-1124-2013 |
|---|---|
| Recall event | 64679 |
| Product | REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Oxford Mlcroplasty Knee System Tibial instrument Tray small surgical hammer supplied with the Oxford Partial Knee Microplasty Instrument set, used for impacting implants. |
| Product code | NRA |
| Recalling firm | Biomet U.K., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2015 |
| FEI number | 3002806535 |
At a glance
- None 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