NA TASCD24Recalls & reported problems
ZimVie US Corp LLC · TSV Angled Screw Channel Driver 24MM · Class 1
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 00844868044741), received between Apr 26, 2023 and Mar 11, 2026 — classified as 1 injury, 17 malfunctions.
The most frequently reported specific device problem is “Fracture” (18 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
- Fracture18
- Separation Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions18
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 11, 2026Fracture
IT WAS REPORTED THAT DRIVER 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 24576102 ↗MalfunctionJan 16, 2026Fracture
IT WAS REPORTED THAT THE DRIVER TIP FRACTURED WHEN TIGHTENING A CROWN AT 30NCM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24091736 ↗MalfunctionDec 5, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23726226 ↗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 22961216 ↗MalfunctionJul 31, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22674245 ↗MalfunctionJul 24, 2025Fracture; Fracture
IT WAS REPORTED; A DRIVER FRACTURED AT THE TIP. NO IMPACT ON THE PATIENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22585156 ↗MalfunctionJun 27, 2025Fracture; Fracture
IT WAS REPORTED THAT THE DRIVER BROKE WHILE COMPLETING A PROCEDURE ON A PATIENT. THEY COMPLETED THE PROCEDURE USING ANOTHER DRIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22345048 ↗MalfunctionJun 13, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22201664 ↗MalfunctionApr 3, 2025Fracture; Fracture
THE DOCTOR REPORTS THAT THE ITEM FRACTURED BY THE TIP. THE PATIENT DID NOT SUFFER ANY NEGATIVE IMPACT ON THEIR HEALTH. PROCEDURE WAS COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21762410 ↗MalfunctionDec 10, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20890088 ↗MalfunctionNov 26, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20786545 ↗MalfunctionNov 20, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20734844 ↗MalfunctionNov 15, 2024Fracture; Fracture
DRIVER BROKEN DURING IMPLANT #46 PLACEMENT. THE TIP OF THE HEXALOBULAR SCREWDRIVER BROKE OFF WHEN THE IMPLANT CROWN WAS PLACED (USING THE CALIBRATED TORQUE KEY). ONLY THE ROUND HEXALOBULAR PART BROKE OFF, FORTUNATELY THE SMALL TIP DID NOT GET STUCK IN THE IMPLANT SCREW. DOCTOR CONFIRMED PROCEDURE COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20694064 ↗MalfunctionNov 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 20641365 ↗MalfunctionSep 20, 2024Fracture; Fracture
THE HEXALOBULAR DRIVER TIP FRACTURED WHEN DOCTOR WAS SCREWING THE TIBASE. THE DOCTOR HAD JUST BOUGHT THE PRODUCT AND IT WAS THE SECOND TIME SHE HAD USED IT. PROCEDURE NOT COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20265294 ↗MalfunctionJun 27, 2024Fracture; Separation Failure; Fracture; Separation Failure
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19621783 ↗InjuryMay 28, 2024Fracture; Fracture
IT WAS REPORTED THAT THE DRIVER TIP BROKE OFF AT 25NCM. THE PATIENT WAS SENT HOME WITH IT ONLY BEING TORQUED AT 25NCM. WILL HAVE THE PATIENT RETURN WHEN NEW DRIVER IS REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19404340 ↗MalfunctionApr 26, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16812666 ↗
Other Accessories, Implant, Dental, Endosseous devices
- N/A 68015189Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous388 reports
- N/A 68015191Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous319 reports
- N/A 68015193Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous283 reports
- N/A 68015187Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous266 reports
- N/A 68015188Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous185 reports
- N/A 68015192Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous159 reports
- N/A 68015190Dentsply Implants Manufacturing GmbH · Accessories, implant, dental, endosseous147 reports
- NobelReplace® 37045Nobel Biocare AB · Accessories, implant, dental, endosseous2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.