FDA Device recall Z-2296-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140
- 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. 6260-9-140 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-2296-2018 |
| 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. 6260-9-140
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 201MJD 20RMJD 20TMED 20XMLE 211MJD 217MKD 21AMKD 21DMKD 21KMJD 21LMKD 21LMKDX1 21VMKD 21WMKD 21WMKDX…Lots 201MJD 20RMJD 20TMED 20XMLE 211MJD 217MKD 21AMKD 21DMKD 21KMJD 21LMKD 21LMKDX1 21VMKD 21WMKD 21WMKDX1 21XMKD 21YMKD 223MAE 234MKE 241MJD 26XMHE 26YMHE 270MHE 280MAE 28TMTD 297MTD 2DDMKE 2DJMJD 2HKMKE 2HNMKE 2JPMKE 2JVMKE 2KKMJD 2MMMAE 2MPMAE 2MRMAE 2MTMAE 2NAMKE 2VDMAE 2VMMAE 2W6MAE 2W6MJD 2W7MJD 2W8MAE 2WAMJD 2WPMHE 2X5MHE 2XTMAE 2XVMAE 301MHE 30PMAE 30XMJD 30YMJD 315MJD 31NMLE 31PMLE 31RMLE 31TMLE 338MAE 33PMED 33RMED 33TMED 33VMED 33WMED 33XMED 343MED 344MED 345MED 361MRA 361MRAX1 362MRA 8E3MMA 8E3MMAX1 8E4MMA 8E6MMA 8E8MMA 8E8MMAX1 8E9MMA 8ERMMA 8H8MPD 8J8MMA 8L6MPD 8NJMMA 8NJMMAX1 8PLMRA 8PMMRA 8PNMRA 8PNMRAX1 8PTMPD 8PXMPD 8T3MMA 8VPMMA 91AMPE 925MLD 926MLD 934MMA 934MMAX1 93DMMA 953MPA 954MPA 954MPAX1 976MMA 977MMA 978MMA 979MMA 97AMMA 97DMMA 97PMTA 97PMTAX1 97RMTA 97TMTA 97VMTA 97WMTA 99EMPE 99HMPE 9ADMME 9AEMME 9AHMME 9AJMME 9AVMPE 9D5MPE 9DMMPE 9DNMMA |
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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-2296-2018%22
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