AVIATOR 48770800Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327273168), received between May 12, 2021 and May 12, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (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.

• MalfunctionMay 12, 2021Mechanical Problem; Material Deformation; Mechanical Problem; Material Deformation

  IT WAS REPORTED THAT DURING INTRA-OPERATIVE FINAL TIGHTENING, 2 AVIATOR RETAINING SCREWDRIVERS COULD NOT 'DRIVE THE SCREW INTO THE POCKING MECHANISM ON THE PLATE'. SURGERY WAS SUCCESSFULLY COMPLETED WITH A 20 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT CAPTURES THE SECOND OF THE TWO SCREWDRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11815518 ↗
• MalfunctionMay 12, 2021Mechanical Problem; Material Deformation; Mechanical Problem; Material Deformation

  IT WAS REPORTED THAT DURING INTRA-OPERATIVE FINAL TIGHTENING, 2 AVIATOR RETAINING SCREWDRIVERS COULD NOT 'DRIVE THE SCREW INTO THE POCKING MECHANISM ON THE PLATE'. SURGERY WAS SUCCESSFULLY COMPLETED WITH A 20 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT CAPTURES THE FIRST OF THE TWO SCREWDRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11815094 ↗