Scorpio 82-7-0908Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327031096), received between Sep 4, 2018 and Dec 10, 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 18, 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.

• InjuryDec 10, 2019Break; Naturally Worn; Break; Naturally Worn

  SURGEON REVISED THE KNEE AS THE PATIENT WAS HYPEREXTENDING. HIS PLAN WAS TO INCREASE POLY THICKNESS AS PATIENT HAS GENERAL LIGAMENT LAXITY. THE SURGEON HAS CONCERNS THAT THE POST HAS BROKEN AND THERE IS WEAR. UPDATE 13/NOVEMBER/2019 WG: AS REPORTED IN THE COMMUNICATION LOG, ORIGINALLY REPORTED BY THE REP: "THE ONLY PRODUCT THAT WAS REVISED WAS THE POLY...THE ITEM REVISED TODAY WAS 827-0908 SCORPIO TIBIAL INSERT SIZE 9, 8MM. THE DOCTOR REPORTS THAT THERE IS WEAR ON THE POLY AND IT IS BROKEN."

  Patient problems: Ambulation or Postural Difficulties; Injury; Joint Disorder

  MAUDE report 9444237 ↗
• InjurySep 4, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT SURGEON PERFORMED A KNEE REVISION - POLY SWAP SURGERY DUE TO PAIN AND DISCOMFORT.

  Patient problems: Injury; Pain

  MAUDE report 7842250 ↗