Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Exprt Precision System: Revision Knee Recalled by Encore Medical, Lp Due to The labeling is missing the size/diameter information.
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 Encore Medical, Lp directly.
Affected Products
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.
Quantity: 209 units
Why Was This Recalled?
The labeling is missing the size/diameter information.
Where Was This Sold?
This product was distributed to 13 states: AL, AZ, AR, CA, CO, FL, GA, MO, NY, OK, RI, SC, WI
About Encore Medical, Lp
Encore Medical, Lp has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report