AESCULAP FF856RRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04038653164523), received between Feb 10, 2021 and Feb 10, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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. How this data works · Data updated Oct 13, 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.

• MalfunctionFeb 10, 2021Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT THERE WAS AN ISSUE WITH FF856R - CASPAR OSTEOPHYTE RONGHV-DTY3MM180MM. ACCORDING TO THE COMPLAINT DESCRIPTION, THE ITEM IS BROKEN (INCIDENT). IT OCCURRED DURING A CERVICAL PROCEDURE AND THERE WERE NO BROKEN PIECES. THERE WAS NO DESCRIBED PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED NOR AVAILABLE / WAS NOT AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11309017 ↗
• MalfunctionFeb 10, 2021Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT THERE WAS AN ISSUE WITH FF856R - CASPAR OSTEOPHYTE RONGHV-DTY3MM180MM. ACCORDING TO THE COMPLAINT DESCRIPTION, THE ITEM IS BROKEN. IT OCCURRED DURING A CERVICAL PROCEDURE AND THERE WERE NO BROKEN PIECES. THERE WAS NO DESCRIBED PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED NOR AVAILABLE / WAS NOT AVAILABLE. THE ADVERSE EVENT / MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11309000 ↗