CONQUEST FN 71179216Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556683620), received between Sep 25, 2020 and Sep 25, 2020 — 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. 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.

• MalfunctionSep 25, 2020Break; Break

  IT WAS REPORTED THAT DURING SURGERY OUTSIDE OF THE PATIENT, THE SCREWDRIVER AND THE EXTENSION ROD BOTH GOT BROKEN, AS WELL AS A MISSING PIECE THAT HOLDS THE SCREW IN BOTH POSITIONS. THERE WAS NO DELAY NOR INJURY REPORTED. A S&N BACKUP DEVICE WAS AVAILABLE TO FINISHED THE SURGERY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10584932 ↗
• MalfunctionSep 25, 2020Break; Break

  IT WAS REPORTED THAT DURING SURGERY OUTSIDE OF THE PATIENT, THE SCREWDRIVER AND THE EXTENSION ROD BOTH GOT BROKEN, AS WELL AS A MISSING PIECE THAT HOLDS THE SCREW IN BOTH POSITIONS. THERE WAS NO DELAY NOR INJURY REPORTED. A S&N BACKUP DEVICE WAS AVAILABLE TO FINISHED THE SURGERY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10584927 ↗