MIS MT-RDL30Recalls & reported problems
MIS Implants Technologies Ltd. · Long hex. drive 0.05 inch · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07290109006987), received between Mar 19, 2026 and Jun 26, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
- Mechanical Problem1
- Separation Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 26, 2026Fracture
IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE DRIVER WAS NOT WORKING PROPERLY DUE TO A BROKEN TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25634944 ↗MalfunctionApr 2, 2026Separation Failure
IT WAS REPORTED THAT THERE WAS A TOOL ISSUE WITH A DEFECTIVE HAND TORQUE DRIVER (MT-RDL30), WHICH CAUSED SIGNIFICANT INCONVENIENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24765224 ↗MalfunctionMar 19, 2026Mechanical Problem
IT WAS REPORTED THAT A LONG SCREWDRIVER (LONG HEX. DRIVE 0.05 INCH) FRACTURED DURING USE WHILE THE DOCTOR WAS PLACING A HEALING CAP. NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24642767 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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