Scorpio 82-7-0710Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327031027), received between Aug 26, 2019 and Aug 26, 2019 — 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

Recent adverse event reports

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

• InjuryAug 26, 2019Device Dislodged or Dislocated; Insufficient Device Problem Information; Device Dislodged or Dislocated; Insufficient Device Problem Information

  THE FIRST SURGERY WAS PERFORMED ON (B)(6) 2019 WITHOUT PROBLEMS. THE PATIENT RETURNS TO THE DOCTOR'S OFFICE WITH PAIN AND DIFFICULTY WALKING. WHEN HE STUDIED, THE X-RAY SHOWED THAT THE INSERT HAD A DIFFERENT ANGULATION THAN NORMAL. REVISION SURGERY IS SCHEDULED ON (B)(6) 2019 AND THE IMPLANT IS REMOVED AND REVISION SURGERY PERFORMED. THE PATIENT IS STABLE. THESE DATA ARE FROM THE DAMAGED INSERT AND IT WAS PUT IN THE FIRST SURGERY CATALOG: 82-7-0708; LOT: TX681R; EXPIRATION: 27-02-2023. THESE DATA ARE FROM THE INSERT THAT WAS CHANGED AND PUT IN THE SECOND SURGERY. THIS INSERT HAS HAD NO PROBLEMS AT THE MOMENT CATALOGUE: 82-7-0710; LOT: 7P7H02; EXPIRATION: 05-03-2023.

  Patient problems: Ambulation or Postural Difficulties; Injury; Pain

  MAUDE report 8932334 ↗