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NA RASD6Recalls & reported problems

ZimVie US Corp LLC · RIGHT ANGLE SLOTTED DRIVER TIP 30MM · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00844868015239), received between Dec 11, 2020 and Dec 11, 2020 — classified as 1 malfunction.

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

  • Fracture1

Patient problems

  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 11, 2020Fracture; Fracture

    IT WAS REPORTED THAT THE DRIVER FRACTURED IN THE TIP. DOCTOR FINISHED THE PROCEDURE USING OTHER INSTRUMENT IN STOCK. TOOTH LOCATION UNKNOWN.

    Patient problems: No Information

    MAUDE report 10990913 ↗

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.