N/A 6179.6008Recalls & reported problems
Globus Medical, Inc. · T8 Driver, SR, 60mm, AO Quick Connect · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889095481594), received between Mar 25, 2024 and Jan 16, 2025 — classified as 1 injury, 1 malfunction.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- Insufficient Information1
- Spinal Column Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 16, 2025Fracture; Fracture
IT WAS REPORTED THAT DURING A CASE, AN ANTHEM T8 DRIVER BROKE AT THE TIP AND IT TOOK AN EXTRA 30MIN TO REMOVE THE SCREW WITH THE TIP STUCK IN IT.
Patient problems: Insufficient Information
MAUDE report 21171877 ↗MalfunctionMar 25, 2024Fracture; Fracture
IT WAS REPORTED THAT DURING A DISTAL RADIUS CASE, AN ANTHEM T8 DRIVER BROKE AT THE TIP WHICH REMAINS IN THE SCREW HEAD POST OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 18971191 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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