FDA Device recall Z-0165-2016
Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replac…
- FDA Device
- Class II
- terminated
- Published 2015-11-04
On 2015-11-04 the FDA classified a Class II recall of Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replac… by Encore Medical, citing the labeling is missing the size/diameter information.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0165-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-09-16 |
| Published | 2015-11-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Encore Medical |
| Distribution | AL, AR, AZ, CA, CO, FL, GA, MO, NY, OK, RI, SC, WI |
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.
Reason
The labeling is missing the size/diameter information.
Identifiers
| code_info | 471T1-001/011; 472T1-000/014; 473T1-000/015; 474T1-000/010; 475T1-000/008 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0165-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.