Scorpio 82-7-0508Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327030969), received between Aug 17, 2018 and Feb 13, 2019 — classified as 2 injuries.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 13, 2019Mechanical Problem; Mechanical Problem

  AT REVISION SURGERY IN (B)(6) 2019, THE POSSIBILITY THAT THE LOCKING POSTERIOR OF THE INSERT WAS OFF BY X-P WAS RECOGNIZED. ADDITIONAL INFO AT (B)(6) 2019: THE REVISION SURGERY IS PLANNED AT (B)(6) 2019. REPORTED UNDER ANOTHER PI FOR THE OTHER KNEE.

  Patient problems: Injury

  MAUDE report 8337675 ↗
• InjuryAug 17, 2018Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT: ADMITTED HYPER EXTENSIBILITY TO PATIENT WHO TOOK TKA IN 2016. THE POST OF THE INSERT WAS BROKEN FROM THE BASE AND THE INSERT WAS REPLACED AT (B)(6) 2018. THE DOCTOR REQUESTED THAT WHAT KIND OF POWER HAS BEEN ADDED AND BROKEN.

  Patient problems: Injury

  MAUDE report 7793804 ↗