CLICKLINE 30310ONSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551121887), received between Jul 29, 2020 and Jul 29, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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

Recent adverse event reports

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

• MalfunctionJul 29, 2020Material Separation; Material Separation

  ALLEGEDLY, PER THE OPERATING ROOM MANAGER, DURING A LAPAROSCOPIC HERNIA PROCEDURE A LARGE PIECE OF PLASTIC "SHEARED OFF " AND FELL INTO THE PATIENT. THE DOCTOR SUCCESSFULLY RETRIEVED THE PIECE WITH NO HARM TO THE PATIENT; PROCEDURE WAS COMPLETED WITH NO ADDITIONAL INTERVENTION.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10338711 ↗