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.
Reported: November 4, 2015 Initiated: September 16, 2015 #Z-0165-2016
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.
Reason for Recall
The labeling is missing the size/diameter information.
Details
- Recalling Firm
- Encore Medical, Lp
- Units Affected
- 209 units
- Distribution
- US Distribution to the states of : SC, WI, RI, NY, MO, AR, OK, GA, FL, AL, CA, AZ and CO.
- Location
- Austin, TX
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Encore Medical, Lp. Units affected: 209 units.
Why was this product recalled? ▼
The labeling is missing the size/diameter information.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 4, 2015. Severity: Moderate. Recall number: Z-0165-2016.
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