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Implant Partners KTCCNP30WDRecalls & reported problems

Microport Orthopedics Inc. · TIB BASE COCR NON POR SZ 5 IMPLANT PARTNERS™ · 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 M684KTCCNP30WD1), received between Feb 15, 2022 and Feb 15, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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

  • Patient-Device Incompatibility1

Patient problems

  • Hypersensitivity/Allergic reaction1

Recent adverse event reports

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

  • InjuryFeb 15, 2022Patient-Device Incompatibility

    ALLEGEDLY, THE PATIENT IS PRESENTING AN ALLERGIC REACTION ON BOTH KNEES.

    Patient problems: Hypersensitivity/Allergic reaction

    MAUDE report 13535645 ↗

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

All Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer devices →

Sources and updates

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