Sentry 161-103Recalls & reported problems
Life Spine, Inc. · T25 SCREWDRIVER · Class 2 · Implant
- 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 00190837034207), received between Jun 9, 2026 and Jun 15, 2026 — 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.
MalfunctionJun 15, 2026Fracture
IT WAS STATED THAT, "THE PART BROKE AS THE DOCTOR WAS USING IT TO TIGHTEN A SCREW WHEN INSTALLING THE PLATE. I COULDN'T SEE INSIDE THE PATIENT WHEN IT HAPPENED BUT I DID SEE HIM ATTEMPT TO TIGHTEN THE SCREW AND HEARD A SNAP AS THE DRIVER TIP BROKE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25511586 ↗MalfunctionJun 9, 2026Fracture
IT WAS STATED THAT, "THE TIP OF THE T25 INSERTER BROKE WHILE ADVANCING ALIF PLATE SCREW."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25443630 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.