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Implant Partners EPI6412RWDRecalls & reported problems

Microport Orthopedics Inc. · PS INSRT IMPL SZ 6 RIGHT 12MM IMPLANT PARTNERS™ · Class 2 · Implant

Data updated Oct 18, 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 M684EPI6412RWD1), received between Jul 1, 2021 and Jul 1, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryJul 1, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    ALLEGEDLY, PATIENT WAS REVISED DUE TO DISASSOCIATION.

    Patient problems: Insufficient Information

    MAUDE report 12101094 ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

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Sources and updates

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