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AMK 1956-45-025Recalls & reported problems

Depuy Orthopaedics, Inc. · AMK TOTAL KNEE SYSTEM TIBIAL INSERT FIXED BEARING CONGRUENCY PS WITH POST SIZE 2 18mm · 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 10603295074397), received between Oct 6, 2017 and Oct 6, 2017 — 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.

  • InjuryOct 6, 2017Naturally Worn; Naturally Worn

    PATIENT WAS REVISED TO ADDRESS POLY WEAR. IT WAS ALSO STATED THAT PATIENT'S PATELLA WAS DISLOCATING, SO SURGEON DECIDED TO DO A SOFT TISSUE PROCEDURE TO GET THE PAYABLE TO TRACK PROPERLY.

    Patient problems: No Information

    MAUDE report 6921573 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

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