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Scorpio 82-7-0308Recalls & reported problems

Howmedica Osteonics Corp. · Tibial Bearing Insert - PS · 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 07613327030877), received between Dec 9, 2020 and Dec 9, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Device Dislodged or Dislocated1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryDec 9, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ON (B)(6) 2020, A FEMALE PATIENT UNDERWENT TKA PROCEDURE (RIGHT). ON AN UNKNOWN DATE, HER KNEE WAS DISLOCATED. ON (B)(6) 2020, REPLACED THE INSERTS. THE REPORTER DOES NOT THINK IT WAS DUE TO A DEFECT OF THE IMPLANT, BUT HE WOULD LIKE TO CONFIRM THE CAUSE IN THE WORN PART.

    Patient problems: Joint Dislocation

    MAUDE report 10978539 ↗

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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