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NA RASH3NRecalls & reported problems

ZimVie US Corp LLC · NARROW RIGHT ANGLE LARGE HEX DRIVER TIP 24MM · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00844868015260), received between Oct 7, 2020 and Sep 16, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Information1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 16, 2022Fracture; Fracture

    IT WAS REPORTED THAT THE SCREWDRIVER FRACTURED WHILE SCREWING THE ABUTMENT INTO THE MOUTH. NO OTHER TOOLS WERE DAMAGED., THE SCREW WAS NOT FRACTURED, ANOTHER SCREWDRIVER WAS USED TO PLACE THE ABUTMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15436291 ↗
  • MalfunctionOct 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: No Information

    MAUDE report 10640811 ↗

Other ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS devices

All ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.