FDA Device recall Z-2298-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-336
- 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. 6260-9-336 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-2298-2018 |
| 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. 6260-9-336
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 20864103 20864104 20904401 20904402 20904403 20904404 20934901 21035401 21035402 21035403 21035404 210…Lots 20864103 20864104 20904401 20904402 20904403 20904404 20934901 21035401 21035402 21035403 21035404 21035405 21164901 21164902 21164903 21164904 21505801 21505802 21505803 21505804 21505805 21686801 21686802 21686803 21686804 21686805 21724101 21724102 22380201 22380202 22380203 22380204 22428103 22428104 22428106 22697601 22697602 22697603 23500101 23500102 23500103 24173601 24269101 24808501 24876201 25290901 25290902 25407001 25448001 26147901 26147902 26380901 27250601 27374701 27374702 27374703 28238601 28281901 28287801 28341901 28341902 29161501 29161502 29273501 30198401 30198402 30198403 30311101 30536301 30536302 92677202A 927MME 92AMME 92DMME 948MME 96419801A 9AKMPE 9D2MPE 9D2MPEX1 9D3MPE 9HLMDA 9HMMDA 9HNMDA A32MLA A33MLA A8HMHA A8VMHA A8XMHA AERMJE AL4MEE AL5MEE AL7MEE AMPMRD ANNMJE AXLMPD AXLMPDX1 D1TMJE D44MPD D45MPD D45MPDX1 D6LMRD D72MRD D79MRD D79MRDX1 E24MHA |
|---|
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-2298-2018%22
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