OSCAR 3 1 (REF OHS2062SU)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 18056099649810), received between Mar 21, 2018 and Mar 21, 2018 — classified as 1 injury.

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

• InjuryMar 21, 2018Mechanical Problem; Mechanical Problem

  THE INFORMATION PROVIDED BY (B)(4) INDICATES: - HOSPITAL NAME: (B)(6). - CONSULTANT IN CHARGE: (B)(6). - INCIDENT NUMBER: (B)(6). - TYPE OF INJURY: NONE. - DATE OF INCIDENT: (B)(6) 2018. - DETAILS OF INCIDENT: TIP OF SINGLE USE OSCAR SCRAPER BROKE OFF INSIDE THE PATIENT'S FEMUR. - ACTION TAKEN: TIP RECOVERED AND SCRAPER DISCARDED FROM USE. (B)(4).

  Patient problems: No Information

  MAUDE report 7356626 ↗