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APEX Revision Knee KP-0455LRecalls & reported problems

Omni Life Science, Inc. · Revision Femur PS, cemented Size 5+ Left · Class 2 · Implant

All models of APEX Revision Knee (22)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841690121220), received between Aug 22, 2019 and Aug 22, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Expiration Date Error” (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

  • Expiration Date Error1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionAug 22, 2019Expiration Date Error

    A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A PRIMARY KNEE SURGERY ON (B)(6) 2019. DURING THE SURGERY AN EXPIRED FEMORAL COMPONENT WAS IMPLANTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8921991 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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