FDA Device recall Z-2299-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
- 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. 6260-9-236 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-2299-2018 |
| 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. 6260-9-236
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 MJHT6N MJHT6T MJK94R MJKAX5 MJKD54 MJKDA6 MJKDD0 MJKDV5 MJKDV7 MJKDV8 MJKE0N MJKE2L MJKE2M MJKE2N M…Lots MJHT6N MJHT6T MJK94R MJKAX5 MJKD54 MJKDA6 MJKDD0 MJKDV5 MJKDV7 MJKDV8 MJKE0N MJKE2L MJKE2M MJKE2N MJKEEV MJKEEW MJKEEY MJKH03 MJKH4W MJKHM4 MJKHM6 MJKHM7 MJKHPT MJKHPW MJKHPX MJKHWJ MJKHXJ MJKJ13 MJKRM4 MJKRNN MJKRT7 MJKT2V MJKTPT MJKTYW MJKV11 MJKV22 MJKVMV MJKVNH MJKVPL MJKVWJ MJKW33 MJM046 MJM0A8 MJM0P9 MJM0WP MJM194 MJM26Y MJM27P MJM2P5 MJM2WT MJM323 MJM33W MJM3HN MJM3NA MJRAKL MJRANR MJRE1T MJRED7 MJREPY MJRH3T MJRH70 MJRH8H MJRHEX MJRJ37 MJRJ60 MJRJ9M MJRJLY MJRJMM MJRK2P MJRKEN MJRKW3 MJRMVA MJRNHN MJRR3N MJRTJ2 MJRTP7 MJRVH0 MJRVMM MJRW0K MJRW87 MJRX01 MJRYMD MJT03J MJT0XL MJT2PD MJT2RP MJT3L3 MJT53H MJT546 MJT5RX MJT6PK MJT6Y3 MJT7DY MJT7RN MJT7V9 MJT8LR MJTEDK MJTEVE MJTHAX MJTHT7 MJTHVP MJTJDA MJTKKM MJTL0N MJTLE6 MJTLR5 MJTMP7 MJTMY5 MJTN0T MJTP1R MJTP4D MJTPE2 MJTR46 MJTRA8 MJTRAP MJTRY7 MJTTKL MJTTT3 MJTV44 MJTVEV MJTVNK MJTVRE MJTVRJ MJTVY8 MJ |
|---|
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-2299-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.