Encore Medical, Lp: Medical Device Recall in 2015 - (Recall #: Z-0165-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: September 16, 2015

Date Posted: November 4, 2015

Recall Number: Z-0165-2016

Event ID: 72216

Reason for Recall:

The labeling is missing the size/diameter information.

Status: Terminated

Product Quantity: 209 units

Code Information:

471T1-001/011; 472T1-000/014; 473T1-000/015; 474T1-000/010; 475T1-000/008

Distribution Pattern:

US Distribution to the states of : SC, WI, RI, NY, MO, AR, OK, GA, FL, AL, CA, AZ and CO.

Voluntary or Mandated:

Voluntary: Firm initiated