MIS CT-SLI10Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07290109005959), received between Jun 16, 2026 and Jul 6, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 6, 2026Fracture

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE TOOL BROKE DURING FIRST USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25715701 ↗
• MalfunctionJun 25, 2026Separation Failure

  IT WAS REPORTED THAT THERE WAS A INSERTION TOOL ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25621392 ↗
• MalfunctionJun 16, 2026Mechanical Problem

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE INSERTION TOOL CANNOT HOLD THE IMPLANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25521038 ↗
• MalfunctionJun 16, 2026Mechanical Problem

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE ISO CONNECTOR ON THE INSERTION INSTRUMENT (CT-SLI10) DOES NOT FIT INTO THE DRILL EXTENSION (MT-DE001).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25520099 ↗