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Lineage 26000010Recalls & reported problems

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

All models of Lineage (35)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684260000101), received between Jul 29, 2020 and Jul 29, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryJul 29, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ALLEGEDLY, RIGHT LEG IS SHORT, CUP IS TOO VERTICAL, PATIENT HAS DISLOCATED 3 TIMES AND THERE IS LUCENCY AROUND THE CUP TO INDICATED THAT IT HAS POOR IN GROWTH. CUP, SCREWS /LINER/HEAD/NECK WERE PULLED. STRYKER CUP WENT IN WITH OUR HEAD AND NECK.

    Patient problems: No Information

    MAUDE report 10341161 ↗

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

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Sources and updates

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