Scorpio 80-4409LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327030327), received between Nov 29, 2018 and Nov 29, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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.

• InjuryNov 29, 2018Unstable; Unstable

  STUDY: TOTAL KNEE REPLACEMENT LEFT SIDE ON (B)(6) 2011. ON (B)(6) 2018 PATIENT REPORTS INSTABILITY DUE TO POSTERIOR CRUCIATE INSUFFICIENCY OF THE LEFT KNEE. KNEE BRACE TO TREAT THE EVENT.

  Patient problems: Injury

  MAUDE report 8117654 ↗

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