Exprt Precision System: Revision Knee — Class II medical device recall Z-0165-2016
Terminated recall by Encore Medical, Lp, reported 2015-11-04, distributed in AL, AR, AZ, CA, CO, FL, GA, MO…. The labeling is missing the size/diameter information.
| Recall number | Z-0165-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, Lp, Austin, TX, United States |
| Recall initiated | 2015-09-16 |
| Classified | 2015-10-26 |
| Reported by FDA | 2015-11-04 |
| Terminated | 2016-01-04 |
| Distributed | AL, AR, AZ, CA, CO, FL, GA, MO, NY, OK, RI, SC, WI |
| Quantity | 209 units |
| Reason classes | labeling |
| Model numbers | 160-010-726/738 |
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 for recall
The labeling is missing the size/diameter information.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0165-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.