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Kyocera Medical Technologies, Inc. A 200Recalls & reported problems

Kyocera Medical Technologies, Inc. · R Tibial Baseplate Cemented Keeled Sz 6 · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841523102136), received between Oct 26, 2016 and Oct 26, 2016.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Markings/Labelling Problem1

Patient problems

  • Not Applicable1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • Oct 26, 2016Device Markings/Labelling Problem; Device Markings/Labelling Problem

    ON (B)(6) 2016, DR. (B)(6) INFORMED DR. (B)(4), PRESIDENT AND CEO OF RENOVIS SURGICAL TECHNOLOGIES, VIA ELECTRONIC MAIL THAT A R TIBIAL BASEPLATE CEMENTED KEELED SZ 8 (LOT #2280-6) WAS LABELED INCORRECTLY AS A R TIBIAL BASEPLATE CEMENTED KEELED SZ 6 (LOT #2280-4) AND IMPLANTED INTO A PATIENT.

    Patient problems: Not Applicable

    MAUDE report 6058024 ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

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Sources and updates

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