NA RASD1Recalls & reported problems
ZimVie US Corp LLC · RIGHT ANGLE SLOTTED DRIVER TIP, 24MM · Class 1
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00844868015215), received between Aug 9, 2021 and Jul 14, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Fracture” (6 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.
Reports received per month
Most reported problems
Device problems
- Fracture6
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 14, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22492461 ↗MalfunctionJul 14, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22492444 ↗MalfunctionJul 9, 2025Fracture; Fracture
IT WAS REPORTED A DRIVER FRACTURE AT THE TIP. NO IMPACT ON THE PATIENT WAS REPORTED. THE PROCESS WAS COMPLETED WITH ANOTHER INSTRUMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22457087 ↗MalfunctionAug 24, 2022Fracture; Fracture
DOCTOR INDICATED CHIPPED TIP, DAMAGED. WHEN REMOVING THE HEALING ABUTMENT, THE DRIVER TIP WAS USED. IT WAS USED FOR THE FIRST TIME, BUT THE TIP PART WAS DAMAGED WITH ALMOST NO TORQUE APPLIED. THE OPERATION HAS BEEN POSTPONED, BUT THERE IS NO HEALTH HAZARD. TOOTH SITE # 29 (UNIVERSAL).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15284994 ↗MalfunctionAug 9, 2021Fracture; Fracture
IT WAS REPORTED THAT THE DRIVER FRACTURED. THE DOCTOR CONFIRMS THAT THE PROCEDURE WAS COMPLETED WITH OTHER INSTRUMENTS AND THAT THE PATIENT DID NOT SUFFER ANY NEGATIVE IMPACT ON HIS HEALTH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12292472 ↗MalfunctionAug 9, 2021Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12292462 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.