CLICKLINE 33310ONRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551134580), received between Jan 11, 2021 and Aug 31, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryAug 31, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  AS PER MANUFACTURER INCIDENT REPORT #(B)(4) RECEIVED FROM THE FACTORY IN (B)(6). IT WAS REPORTED THAT THERE WAS AN ISSUE WITH THE FORCEPS INSERT. ACCORDING TO THE COMPLAINT DESCRIPTION, THE DEVICE WAS USED DURING LAPAROSCOPIC CASE. WHILE IN USE, THE INSTRUMENT NICKED A SECTION OF THE BOWEL, CREATING A SMALL TEAR.

  Patient problems: Bowel Perforation

  MAUDE report 15330236 ↗
• MalfunctionJan 11, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

  AS PER A COPY OF A MIR WE RECEIVED FROM THE FACTORY IN (B)(6): THE INSTRUMENT HAS BEEN USED TO MOBILIZE THE UTERINE GRAFT. AT THE END OF THE OPERATION, A MILLIMETER PIECE OF THE DISTAL BRANCH OF THE FORCEPS IS MISSING, CONFIRMED WITH CONTROL X-RAY. THE PATIENT WAS INFORMED.

  Patient problems: Foreign Body In Patient

  MAUDE report 11151514 ↗