Arsenal 87013Recalls & reported problems
Alphatec Spine, Inc. · T25 SELF RETAINING DRIVER · Class 1
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00844856069589), received between Sep 25, 2018 and Dec 16, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (5 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
- Break5
- Material Separation2
- Entrapment of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 16, 2025Break; Material Separation; Break; Material Separation
IT WAS REPORTED THAT THE TIP OF THE DRIVER IS TWISTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817346 ↗MalfunctionAug 12, 2025Break; Break
IT WAS REPORTED THAT THE DRIVER BROKE DURING A CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22788007 ↗MalfunctionApr 2, 2025Break; Material Separation; Break; Material Separation
IT WAS REPORTED THAT THE DRIVER WAS BEING USED TO REMOVE PREVIOUSLY IMPLANTED HARDWARE WHEN THE TIP BROKE OFF INTO THE SET SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21754429 ↗MalfunctionFeb 19, 2025Break; Break
IT WAS REPORTED THAT THE DRIVER BROKE DURING A SCREW REMOVAL SURGERY. NO PIECES OF THE BROKEN DRIVER WERE LEFT IN THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21414739 ↗MalfunctionSep 25, 2018Break; Entrapment of Device
WHILE INSERTING THE SCREW INTO THE PEDICLE, THE TIP OF THE T25 DRIVER BROKE OFF IN THE HEAD OF THE SCREW. THE SURGERY WAS COMPLETED SUCCESSFULLY. EVERYTHING WAS REMOVED FROM THE PATIENT AND THE PATIENT WAS NOT HARMED IN THE PROCESS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7906614 ↗
Other SCREWDRIVER devices
- DELTA XTEND 2307-92-003Depuy (Ireland) · SCREWDRIVER751 reports
- EXPEDIUM 279712400Medos International Sàrl · SCREWDRIVER551 reports
- NA 314.467Synthes GmbH · SCREWDRIVER498 reports
- N/A 5584111Medtronic Sofamor Danek, Inc. · SCREWDRIVER492 reports
- QUICKSET 2274-47-000Depuy (Ireland) · SCREWDRIVER487 reports
- NA 03.130.010Synthes GmbH · SCREWDRIVER1 recall422 reports
- QUICKSET 2274-63-000Depuy (Ireland) · SCREWDRIVER404 reports
- EVOS 71175072Smith & Nephew, Inc. · SCREWDRIVER336 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.