NA TASCD30Recalls & reported problems
ZimVie US Corp LLC · TSV Angled Screw Channel Driver 30MM · Class 1
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00844868044758), received between Jul 8, 2024 and Mar 11, 2026 — classified as 1 injury, 12 malfunctions.
The most frequently reported specific device problem is “Fracture” (13 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
- Fracture13
Patient problems
- No Clinical Signs, Symptoms or Conditions13
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 11, 2026Fracture
IT WAS REPORTED THAT THE DRIVER BOTH BROKE DURING SEATING OF THE SCREW FOR AN ANGLED TI BASE. PATIENT WAS NOT AFFECTED, ANOTHER DRIVER WAS USED TO COMPLETE PROCEDURE. NO FURTHER INFORMATION PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24571055 ↗MalfunctionMar 5, 2026Fracture
THE DOCTOR REPORTS THAT THE DRIVER FRACTURED DURING USE AT 30 NEWTONS AT THE TIP OF THE HEAD. THE PROCEDURE WAS COMPLETED USING ANOTHER DRIVER, WITH NO NEGATIVE IMPACT ON THE PATIENT¿S HEALTH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24516839 ↗MalfunctionFeb 10, 2026Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24302380 ↗MalfunctionNov 17, 2025Fracture; Fracture
THE DOCTOR REPORTED THAT DURING THE TRY-IN OF A SCREW-RETAINED ABUTMENT ON THE IMPLANT, THE EXTRA-LOBULAR DRIVER BROKE AT THE NECK LEVEL. THERE WAS A DELAY IN PLACING THE CROWN. DOCTOR HAD TO WAIT FOR A SCREWDRIVER BORROWED FROM THE PROSTHETIST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23568089 ↗MalfunctionOct 20, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23335277 ↗MalfunctionSep 4, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22961149 ↗MalfunctionSep 4, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22961132 ↗MalfunctionAug 18, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22827087 ↗MalfunctionJul 4, 2025Fracture; Fracture
THE DOCTOR REPORTS THAT WHEN APPLYING 30 NEWTONS OF FORCE DURING CROWN PLACEMENT, THE DRIVER FRACTURED AT THE TIP. THE FRACTURED TIP WAS RETRIEVED ALONG WITH THE DRIVER. PROCEDURE WAS COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22403333 ↗MalfunctionJul 1, 2025Fracture; Fracture
IT WAS REPORTED THE DRIVER FRACTURED AT THE TIP AFTER THE SECOND USE. PATIENT WILL RETURN TO COMPLETE THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22368921 ↗MalfunctionApr 17, 2025Fracture; Fracture
THE DOCTOR REPORTS THAT THE TIP OF THE SCREWDRIVER FRACTURED. PROCEDURE WAS COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21854856 ↗InjurySep 23, 2024Fracture; Fracture
IT WAS REPORTED THAT THE DRIVER HAD A FRACTURED TIP. THE PATIENT HAD TO BE RESCHEDULED WITH THE PERIODONTIST WHO PLACED THE IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20284167 ↗MalfunctionJul 8, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19687451 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.