Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due to A femoral component containing pegs was found in...
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 Ortho Development Corporation directly.
Affected Products
PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total knee arthroplasty procedures.
Quantity: 5
Why Was This Recalled?
A femoral component containing pegs was found in a box for the pegless version.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ortho Development Corporation
Ortho Development Corporation has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report