Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis — Class II medical device recall Z-1266-2015
Terminated recall by Zimmer, Inc., reported 2015-03-18, distributed in AK, AL, AZ, CA, CO, FL, IL, IN…. An increase in complaints of loosening and radiolucent lines.
| Recall number | Z-1266-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2015-01-28 |
| Classified | 2015-03-12 |
| Reported by FDA | 2015-03-18 |
| Terminated | 2018-03-13 |
| Distributed | AK, AL, AZ, CA, CO, FL, IL, IN, KS, MA, ME, MI, MN, MO, NC, NJ, NV, NY, OH, OK, PA, SD, TN, TX, UT, VA, WA, WI |
| Countries outside the US | AE, AT, AU, BE, CA, CH, DE, IT, KR, LB, LU, NL, NZ, SE, ZA |
| Quantity | 11,658 |
Product
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer For use in either posterior cruciate retaining or sacrificing surgical procedures.
Reason for recall
An increase in complaints of loosening and radiolucent lines.
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-1266-2015. 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.