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Kyocera Medical Technologies, Inc. A 400Recalls & reported problems

Kyocera Medical Technologies, Inc. · Tapered Femoral Stem, Std Offset, 10.5mm · 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 00841523102549), received between Feb 19, 2022 and Feb 19, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Expiration Date Error” (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

  • Expiration Date Error1

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.

  • MalfunctionFeb 19, 2022Expiration Date Error; Expiration Date Error

    EXPIRED IMPLANT WAS USED IN SURGERY ON (B)(6) 2022. IMPLANT EXPIRED ON 10/13/2021. IMPLANTATION WAS AN OVERSIGHT FROM BOTH THE SURGICAL REP. AND THE NURSE IN SURGERY WHO CALL OUT THE ITEMS BEING IMPLANTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13565125 ↗

Other Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented devices

All Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented devices →

Sources and updates

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