FDA Device recall Z-1266-2015
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coat…
- FDA Device
- Class II
- terminated
- Published 2015-03-18
On 2015-03-18 the FDA classified a Class II recall of Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coat… by Zimmer, citing an increase in complaints of loosening and radiolucent lines.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1266-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-28 |
| Published | 2015-03-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | AK, AL, AZ, CA, CO, FL, GA, IL, IN, KS, LA, MA, ME, MI, MN, MO, NC, NJ, NV, NY, OH, OK, PA, SD, TN, TX, UT, VA, WA, WI |
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
An increase in complaints of loosening and radiolucent lines.
Identifiers
| code_info | All lots and sizes; Sizes C-J Left and Right. |
|---|
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-1266-2015%22
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