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INTERSEAL® 30153258Recalls & reported problems

Microport Orthopedics Inc. · INTERSEAL® DURAMER® ACETABULAR C-LINER 32mm 15° GROUP 3 STD · 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 M684301532581), received between May 22, 2020 and May 22, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn1

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.

  • InjuryMay 22, 2020Naturally Worn; Naturally Worn

    ALLEGEDLY THE POLY IS WORN. ADDITIONAL INFORMATION: DISLOCATING ON (B)(6) 1998.

    Patient problems: No Information

    MAUDE report 10083061 ↗

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

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Sources and updates

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