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Scorpio 72-12-0910Recalls & reported problems

Howmedica Osteonics Corp. · Cruciate Retaining Tibial Insert · Class 2 · Implant

All models of Scorpio (107)

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 07613327044485), received between Oct 4, 2018 and Oct 4, 2018 — 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 18, 2026.

Most reported problems

Device problems

  • Naturally Worn1

Patient problems

  • Inadequate Osseointegration1
  • Inflammation1
  • Injury1
  • Osteolysis1

Recent adverse event reports

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

  • InjuryOct 4, 2018Naturally Worn; Naturally Worn

    AS REPORTED: "REVISION OF LEFT TOTAL KNEE DUE TO SUBSIDED TIBIAL TRAY". UPDATE 10/04/2018: DIAGNOSIS OF "MARKED OSTEOLYSIS PROXIMAL MEDIAL TIBIA WITH LOOSE TIBIAL COMPONENT AND SYNOVITIS".

    Patient problems: Inadequate Osseointegration; Inflammation; Injury; Osteolysis

    MAUDE report 7936260 ↗

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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