Skip to content

Lineage 26000014Recalls & reported problems

Microport Orthopedics Inc. · CERAMIC FEMORAL HEAD 36mm SLT TAPER MEDIUM NECK · Class 3 · Implant

All models of Lineage (35)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684260000141), received between Apr 26, 2023 and Apr 26, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Packaging Problem” (2 reports).

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 16, 2026.

Most reported problems

Device problems

  • Packaging Problem2
  • Unsealed Device Packaging1

Patient problems

  • Insufficient Information2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 26, 2023Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem

    ALLEGEDLY, INNER SEAL OF PRODUCT NOT SEALED/NOT STERILE. PRODUCT USED.

    Patient problems: Insufficient Information

    MAUDE report 16815748 ↗
  • InjuryApr 26, 2023Packaging Problem; Packaging Problem

    ALLEGEDLY, INNER PACKAGE WAS NOT SEALED. PRODUCT WAS USED.

    Patient problems: Insufficient Information

    MAUDE report 16815503 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page