T.L.I.F. 202711002Recalls & reported problems
Medos International Sàrl · T.L.I.F. SG INSTRUMENTS CUP CURETTE, UP ANGLED 8mm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034184180), received between May 11, 2023 and May 11, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 11, 2023Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN AUSTRALIA AS FOLLOWS: IT WAS REPORTED THAT UPON INSPECTION ON (B)(6) 2023, THE INSTRUMENT WAS CRACKED, AND THE HANDLE SNAPPED IN HALF AT THE POINT OF THE CRACK. THIS WAS IDENTIFIED BY THE LOAN KIT TECHNICIAN DURING INSPECTION. NO PATIENT OR PROCEDURE INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE T.L.I.F. SG INSTRUMENTS CUP CURETTE, UP ANGLED 8MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16911246 ↗
Other CURETTE devices
- Centurion I68470Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 66745Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68040Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68380Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67050Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68340Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I67970Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68480Centurion Medical Products Corporation · CURETTE1 recall0 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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