Biomet U.K., Ltd.
5 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Ox recall (Z-1124-2013) | Biomet U.K., Ltd. | 2013-04-15 |
| Oxford Gap Gauge SML 3/4mm. The instrument is used for an intermediate check of the flexio recall (Z-2224-2012) | Biomet U.K., Ltd. | 2012-08-17 |
| Vanguard Knee Instrumentation Distal Cutting Block without Handles, REF 32-487002 LOT 2561 recall (Z-1222-2012) | Biomet U.K., Ltd. | 2012-03-19 |
| Vanguard Knee Instrumentation Tibial Resection Tower Universal with alignment tower geomet recall (Z-1223-2012) | Biomet U.K., Ltd. | 2012-03-19 |
| Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UN recall (Z-2698-2011) | Biomet U.K., Ltd. | 2011-06-29 |
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Every clearance here is in the API, with alerts when new ones post.