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INTERSEAL® 50152858Recalls & reported problems

Microport Orthopedics Inc. · INTERSEAL® DURAMER® ACETABULAR C-LINER 15° +4mm 28mm ID GRP 3 · Class 2 · Implant

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 M684501528581), received between Feb 1, 2021 and Feb 1, 2021 — 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

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryFeb 1, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ALLEGEDLY, PATIENT KEEPS DISLOCATING (3 TIMES SINCE 12/19). LINER WAS SWAPPED OUT FOR A 32MM HEAD AND 32MM LINER.

    Patient problems: Joint Dislocation

    MAUDE report 11263063 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices →

Sources and updates

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