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Encore Medical, Lp recalls Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee
Recalled November 4, 2015 · FDA recall Z-0165-2016 · Encore Medical
Hazard
The labeling is missing the size/diameter information. · FDA Class II
Units
209 units
Sold at
US Distribution to the states of : SC, WI, RI, NY, MO, AR, OK, GA, FL, AL, CA, AZ and CO.
Description
The labeling is missing the size/diameter information.
Product
Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replace the native patella.
Manufacturer(s)
Encore Medical, Lp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →