Citation TMZF HA Hip Stem Right (Femoral Hip Prosthesis) Catalog No. 6265-5116
FDA Recall Z-0349-03 · Posted 2002-12-19
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Recalling FirmHowmedica Osteonics Corp
Recall StatusTerminated
Product CodeMEH
Date Initiated2002-11-12
Date Terminated2003-04-04
Product Quantity16
Reason for Recall
Hip Stem Fractures in the neck area.
Firm Action
Letters to Surgeons was sent certified mail on Nov. 4, 2002. Letters to Howmedica agents send on Nov. 12, 2002.
Root Cause
Other
Distribution Pattern
Product was distributed to hospitals and Howmedica Branch reps throughout the US.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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