NA ASCDT24Recalls & reported problems
ZimVie US Corp LLC · ANGLED SCREW CHANNEL 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 00844868044017), received between Oct 24, 2022 and Oct 16, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 16, 2024Fracture; Fracture
IT WAS REPORTED THAT THE DOCTOR TORQUED DOWN ON A GOLD SCREW ALL THE WAY AND THE TIP OF THE DRIVER BROKE OFF INSIDE OF THE GOLD SCREW. THE DOCTOR WAS UNABLE TO REMOVE THE BROKEN TIP FROM THE SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20464729 ↗MalfunctionOct 24, 2022Fracture; Fracture
IT WAS REPORTED THAT THE ANGLED DRIVER BROKE DURING TORQUING. PROCEDURE WAS COMPLETED USING ANOTHER DRIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15663286 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.