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Kyocera Medical Technologies, Inc. S 141Recalls & reported problems

Kyocera Medical Technologies, Inc. · Tesera ST, 25mm X 11mm X 10mm, Convex, T3 · 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 00841523134168), received between Jun 22, 2023 and Jun 22, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Labelling, Instructions for Use or Training 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

  • Labelling, Instructions for Use or Training Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 22, 2023Labelling, Instructions for Use or Training Problem; Labelling, Instructions for Use or Training Problem

    AN EXPIRED IMPLANT WAS USED IN SURGERY ON (B)(6) 2023. THE IMPLANT EXPIRED ON (B)(6) 2023. DURING THE PROCEDURE, THE SALES REPRESENTATIVE NOTIFIED THE SURGEON OF THE EXPIRED IMPLANT; HOWEVER, THE SURGEON WAS COMFORTABLE WITH LEAVING THE IMPLANT IN THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17187858 ↗

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Sources and updates

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