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FDA product code LKH · Class 1 · Microbiology
1
Registered devices
0
Adverse events
6
Recalls
8
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
| 2006-08-15 | Encore Medical, Lp | Complaints received that device used to prepare femur to receive femoral implant would split during surgery. |
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