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ENDOPATH 23NBLRecalls & reported problems

Ethicon Endo-Surgery, LLC · Endopath Bladeless Trocars with Smooth Sleeves · Class 2

All models of ENDOPATH (37)

Data updated Oct 16, 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 10705036000396), received between Feb 24, 2020 and Feb 24, 2020 — 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 16, 2026.

Most reported problems

Device problems

  • Break1
  • Material Separation1

Patient problems

  • No Code Available1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 24, 2020Break; Material Separation; Material Separation

    IT WAS REPORTED THAT DURING A LAPAROSCOPIC APPENDECTOMY, THE DOCTOR PULLED THE INTRODUCER OUT OF THE TROCAR AND WHILE MANIPULATING TISSUE, THE CANNULA OF THE TROCAR BROKE IN THE MIDDLE OF THE CANNULA. THE DOCTOR DECIDED TO CONVERT TO OPEN TO REMOVE THE TROCAR AND COMPLETE THE PROCEDURE.

    Patient problems: No Code Available; No Consequences Or Impact To Patient

    MAUDE report 9748168 ↗

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Sources and updates

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