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Ortho Development Corporation recalls PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision
Recalled May 21, 2014 · FDA recall Z-1610-2014 · Ortho Development
Hazard
A femoral component containing pegs was found in a box for the pegless version. · FDA Class II
Units
5
Sold at
US Nationwide Distribution in the states of NV, and AZ.
Description
A femoral component containing pegs was found in a box for the pegless version.
Product
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.
Manufacturer(s)
Ortho Development Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →