FDA Device recall Z-2293-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
- FDA Device
- Class II
- terminated
- Published 2018-07-11
On 2018-07-11 the FDA classified a Class II recall of LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040 by Howmedica Osteonics, citing the recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2293-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-22 |
| Published | 2018-07-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Howmedica Osteonics |
| Distribution | US |
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Reason
The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011.
Identifiers
| code_info | Lots 586MTA 587MTA 588MTA 588MTAX1 589MTA 5E8MMD 5E9MMD 5EAMMD 5HDMDE 5JKMMD 5JKMMDX1 5L9MPA 5LHMPA 5LJMP…Lots 586MTA 587MTA 588MTA 588MTAX1 589MTA 5E8MMD 5E9MMD 5EAMMD 5HDMDE 5JKMMD 5JKMMDX1 5L9MPA 5LHMPA 5LJMPA 5LVMPA 5LVMPAX1 5LWMPA 5LXMPA 5MPMTD 5MRMTD 5MRMTDX1 5R0MND 5TDMMD 5V1MND 5V7MHD 5VHMHD 5VTMHD 5W0MHD 5WEMHD 5WKMHD 5WNMHD 5WTMHD 5WVMAE 5WXMAE 5WYMAE 5X0MAE 60RMAE 61DMME 61EMME 61HMME 61HMND 61JMME 61KMDE 61LMDE 61LMDEX1 61MMDE 62HMND 62HMNDX1 62LMMD 63YMAD 63YMADX1 640MAD 641MAD 642MAD 650MDE 65NMMD 662MMD 662MND 665MND 68PMMD 690MED 691MED 692MED 693MED 69DMTD 6A9MTD 6ARMAD 6HNMMD 6HYMAD 6J2MAD EJAMHE EJTMME EJVMME EK2MME EKLMDD EL3MME ENNMRD ETTMPA ETXMPA EVLMDD EXRMRD EXTMRA EXVMRA EXVMRAX1 EY1MRD H0PMHE H0RMDD H0TMTD H0VMTD H0WMTD H0XMTD H0YMTD H16MDD H16MDDX1 H21MHE H36MJE H36MJEX1 H37MJE H38MJE H39MJE H3HMHE H50MRD H51MRD H52MRD H79MHE H90MTD H91MTD H92MTD H9RMTD H9TMTD HH6MHE HHLMMA HHLMMAX1 HHMMMA HHNMMA HHPMMA HHRMMA HHRMMAX1 HJ4MAE HJ5MAE HJ6MAE HJ |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2293-2018%22
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