FDA Device recall Z-2294-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
- 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. 6260-9-044 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-2294-2018 |
| 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. 6260-9-044
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 3P9MKE 3PEMKE 3PHMKE 3PJMKE 3PKMKE 3XJMKE 3XKMKE 44EMJD 44HMJD 44JMJD 46NMRA 46PMRA 46PMRAX1 46RMRA…Lots 3P9MKE 3PEMKE 3PHMKE 3PJMKE 3PKMKE 3XJMKE 3XKMKE 44EMJD 44HMJD 44JMJD 46NMRA 46PMRA 46PMRAX1 46RMRA 485MJD 487MJD 488MJD 48AMJD 48EMJD 4A5MJD 4A5MJDX1 4DYMHE 4E2MHE 4E3MHE 4E4MHE 4KPMTD 4Y2MTD 4Y3MTD 4Y4MTD 54KMJD 54LMJD 54MMJD 67VMLE 6D7MLE 6DPMLE 6DXMLE 6K3MKE 6LHMKE 6LLMKE 6LMMKE 6LNMKE 6NMMKE 6R1MKE 7AJMRA 7AJMRAX1 7AKMRA 7AKMRAX1 803MMD 805MMD 806MMD 807MMD 807MMDX1 80AMMD 80DMMD 85MMPA 85NMPA 85PMPA 8J0MPA 8Y6MRD 918MRD 91RMRD 92XMND 939MND 93HMND 94VMPA 94XMPA 94XMPAX1 9JMMRD 9KKMRD 9T3MPD MHH6ML MHH6VE MHH728 MHJ39H MHJ3JR MHJ3K9 MHJ3NE MHK4AJ MHK4RV MHK53A MHK53E MHK54J MHK54K MHK5AD MHK5DJ MHKL67 MHKL7R MHKLP2 MHKLP4 MHKLTD MHKLTE MHKLVL MHKLWD MHKLXJ MHKM15 MHKME5 MHKMT6 MHKMY0 MHKN2A MHKN4T MHKN70 MHKND1 MHKNR0 MHKNR6 MHKNRX MHKNTY MHKNV0 MHKNV1 MHLPVJ MHLR02 MHLR0D MHLR0J MHLR0L MHLR4J MHLR60 MHLR61 MHLR62 MHLRK5 MHLRTL MHLRTP MHLRTT MHLRTW MHLT1 |
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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-2294-2018%22
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