FDA Device recall Z-2297-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144
- 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. 6260-9-144 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-2297-2018 |
| 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. 6260-9-144
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 869MPA 869MPAX1 87PMKD 8A3MKD 8A3MKDX1 8ARMRD 8DTMKD 8EVMRD 8EVMRDX1 8KRMPA 8KRMPAX1 8M2MRD 8RVMRD 8…Lots 869MPA 869MPAX1 87PMKD 8A3MKD 8A3MKDX1 8ARMRD 8DTMKD 8EVMRD 8EVMRDX1 8KRMPA 8KRMPAX1 8M2MRD 8RVMRD 8TDMPA 8TDMPAX1 8TTMPD 8V6MPD 8V9MPD 8V9MPDX1 8VVMPD 8X1MPD 900MPD 913MPD 938MPD 938MPDX1 94JMLD 94YMPA 94YMPAX1 94YMPAX2 9LHMLD 9M3MLD 9R2MAD 9R2MADX1 9R4MAD 9R5MAD 9R5MLA 9R6MAD 9R7MAD 9R7MADX1 9RMMLA 9RYMLA 9RYMLAX1 9TEMLA 9V9MRA 9VAMRA 9VDMRA 9VDMRAX1 9VEMRA 9YYMPD 9YYMPDX1 A00MPD A00MPDX1 A08MPD A09MPD A09MPDX1 A2EMEE A2HMEE A2JMEE A2KMEE A4DMLD A53MEE A5AMLA A5DMLA A5HMLA A6XMEE A77MLD A94MEE AA1MLD AA2MTA AA2MTAX1 MHDY1K MHDY28 MHDY28X1 MHDY2D MHE0N7 MHE0TW MHE0W3 MHE0W3X1 MHE0WL MHE10K MHE10X MHE118 MHE11A MHEKK3 MHEKME MHEKVT MHEKVTX1 MHEKW5 MHEKW5X1 MHEL3L MHEL3Y MHEL3YX1 MHEL4D MHEL4R MHEL4RX1 MHEL80 MHEL80X1 MHEL8D MHEL8DX1 MHELD9 MHELD9X1 MHELK6 MHEM74 MHH4EX MHH4EXX1 MHH4LW MHH4W7 MHH514 MHH53R MHH549 MHH54A MHH54D MHH54E MHH55W MHH55WX1 MHH55X MHH5DR MH |
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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-2297-2018%22
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