Scorpio 80-4405RRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327030303), received between Jun 8, 2022 and Jun 8, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (1 report).

1 other recall cover devices cleared under the same FDA submission (K042343); they may or may not involve this specific model.

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

Recent adverse event reports

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

• InjuryJun 8, 2022Unstable; Osseointegration Problem; Migration; Unstable; Osseointegration Problem; Migration

  ASEPTIC MOBILIZATION OF THE PROSTHESIS. REASON THE DEVICE WAS USED: RIGHT KNEE OSTEOARTHRITIS. TOTAL RIGHT KNEE REPLACEMENT. YEAR OF IMPLANT: 2017.

  Patient problems: Arthritis; Insufficient Information

  MAUDE report 14634103 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042343. One submission often covers many models, so check the product and lot details in each record.

• Z-1634-2015 · Aug 15, 2014 · Terminated
  Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of