Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due to The recalling firm has received a higher than...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Howmedica Osteonics Corp. directly.
Affected Products
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report