FDA Device recall Z-2292-2018
LFIT Anatomic CoCr Femoral Heads, 6260-9-036
- 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, 6260-9-036 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-2292-2018 |
| 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, 6260-9-036
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 10176601 10176602 10446901 10852601 10937801 11121001 11121002 11969801 11969802 12204501 12204502 12…Lots 10176601 10176602 10446901 10852601 10937801 11121001 11121002 11969801 11969802 12204501 12204502 12204503 12668301 12668302 12668303 13365101 13365102 13365103 14101701 14101702 14390201 14390202 15186701 15186702 15186703 15292201 15341301 15629301 15759301 16462501 16575502 16637001 16666801 16684301 17158901 17158902 17230301 17230302 18133801 18133802 18133803 18216101 18216102 18216103 18783601 18783602 19313601 19313602 19313603 19313604 19506101 19506102 19549501 19549502 19614801 19614802 19614803 19691301 19691302 19715701 19738101 19738102 19738103 19780201 19780202 19843901 19843902 20167601 20479101 20479102 35007304 35246401 35826901 35826902 35826903 35826904 35826905 36140401 36140402 36140403 36140404 36140405 36467201 36467202 36467203 36467204 36993801 37014601 37014602 37014603 37014604 37014605 37034301 37034302 37252501 37252502 37252503 37367101 37367102 373 |
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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-2292-2018%22
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