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Scorpio 72-12-0508Recalls & reported problems

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

All models of Scorpio (107)

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 07613327044331), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Degraded” (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

  • Degraded1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryJul 11, 2022Degraded; Degraded

    PATIENT ADMITTED WITH KNEE PAIN FOR A SCOPE AND ASPIRATE OF KNEE JOINT. WHEN CLEARING UP THE KNEE, THE SURGEON NOTICED A DEFICIT IN THE POLY ON THE POSTERIOR MEDIAL PORTION. HE COULD SEE THE RIM OF THE BASEPLATE SO KNEW IT WAS DELAMINATED/SHEARED IN HIS WORDS.

    Patient problems: Pain

    MAUDE report 14982978 ↗

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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