T.L.I.F. 274279000Recalls & reported problems
Depuy Spine, LLC · T.L.I.F. INSTRUMENTATION CHISEL, STRAIGHT 8mm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10705034191874), received between Jul 12, 2018 and Jul 12, 2018 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (6 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 18, 2026.
Most reported problems
Device problems
- Material Deformation6
- Defective Component1
Patient problems
- No Known Impact Or Consequence To Patient7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682787 ↗MalfunctionJul 12, 2018Defective Component
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682754 ↗MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682703 ↗MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682656 ↗MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682631 ↗MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682600 ↗MalfunctionJul 12, 2018Material Deformation; Material Deformation
TIP OF CHISEL DEFECTIVE AFTER FIRST USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7682579 ↗
Other CHISEL, SURGICAL, MANUAL devices
- SIGMA 2024-85-000Depuy (Ireland) · CHISEL, SURGICAL, MANUAL63 reports
- NA 2421-01-000Depuy (Ireland) · CHISEL, SURGICAL, MANUAL36 reports
- NA 399.56Synthes GmbH · CHISEL, SURGICAL, MANUAL11 reports
- NA 399.55Synthes GmbH · CHISEL, SURGICAL, MANUAL10 reports
- NA 332.121Synthes GmbH · CHISEL, SURGICAL, MANUAL5 reports
- INSTRUMENT 6541-4-709Howmedica Osteonics Corp. · CHISEL, SURGICAL, MANUAL4 reports
- NA 202953Depuy Spine, LLC · CHISEL, SURGICAL, MANUAL4 reports
- GENESIS II 71440144Smith & Nephew, Inc. · CHISEL, SURGICAL, MANUAL3 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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