FDA Device recall Z-2295-2018
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136
- 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. 6260-9-136 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-2295-2018 |
| 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. 6260-9-136
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 13461301 13461302 14097201 14097202 14390101 14390102 14814301 14934401 14941101 14973401 15029001 150…Lots 13461301 13461302 14097201 14097202 14390101 14390102 14814301 14934401 14941101 14973401 15029001 15029002 15186801 15186802 15186803 15341401 15341402 15341403 15341404 15629401 15629402 15759601 16462601 16551101 16551102 16575601 16575602 16644801 16666901 16684501 17159001 17159002 17230201 17230202 18077901 18110901 18110902 18110903 18216001 18216002 18216003 18298901 18298902 18744901 18748501 18748502 18783701 18783702 18783703 19122001 19122002 19362201 19362401 19362501 19362601 19506201 19506202 19549601 19549602 19634101 19634102 19634103 19634104 19691001 19691002 19696801 19696802 19696803 19716501 19719801 22400903 22400904 22402901 22407101 22648401 22648402 22648403 22740701 22740702 22740703 22740704 22740705 22775201 22775202 22775203 22775204 22775205 22817801 23434501 23434502 23434503 23471701 23516001 23516002 23516003 23542801 23542802 23542803 24109201 2412 |
|---|
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-2295-2018%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.