CLICKLINE 33310CCRecalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 04048551134108), received between Nov 4, 2024 and Sep 21, 2026 — classified as 6 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 21, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50848637 ↗
• InjuryJul 27, 2026Detachment of Device or Device Component

  It was reported that "There is a possibility that two lock pins from the product in question fell into the abdominal cavity. It is believed that they fell out when the omentum was grasped at the end of the surgery. An X-ray examination was performed, but the damaged area was not found. Another X-ray examination is scheduled."

  Patient problems: Foreign Body In Patient

  MAUDE report 50008551 ↗
• InjuryJul 27, 2026Detachment of Device or Device Component

  It was reported that "There is a possibility that two lock pins from the product in question fell into the abdominal cavity. It is believed that they fell out when the omentum was grasped at the end of the surgery. An X-ray examination was performed, but the damaged area was not found. Another X-ray examination is scheduled."

  Patient problems: Foreign Body In Patient

  MAUDE report 50008328 ↗
• InjuryMay 22, 2026Patient Device Interaction Problem

  IT WAS REPORTED WHILE USING THE 33310CC, THE DOCTOR TORE THE INTESTINE AND CAUSED BLEEDING WHEN GRASPING INTESTINAL TISSUE. INSTRUMENT INSPECTION REVEALED THAT THE PRODUCT SURFACE WAS ROUGH, WHICH IS PRONE TO CAUSING INTESTINAL TISSUE BLEEDING DURING GRASPING. FURTHERMORE IT WAS STATED IT IS INTESTINAL TISSUE INJURY. THE CLINICIAN BELIEVES THAT THE INJURY MAY ALSO BE RELATED TO THE PATIENT'S ADVANCED AGE AND FRAGILE INTESTINAL TISSUE, BUT THIS CANNOT BE CONFIRMED. MOREOVER, RC INSPECTION REVEALED THAT THE DEVICE SURFACE WAS NOT SIGNIFICANTLY ROUGH. THE SURGEON PROMPTLY PERFORMED SUTURING ON THE LACERATED BOWEL TISSUE.

  Patient problems: Laceration(s)

  MAUDE report 25260828 ↗
• InjuryMay 22, 2026Patient Device Interaction Problem

  IT WAS REPORTED WHILE USING THE 33310CC, THE DOCTOR TORE THE INTESTINE AND CAUSED BLEEDING WHEN GRASPING INTESTINAL TISSUE. INSTRUMENT INSPECTION REVEALED THAT THE PRODUCT SURFACE WAS ROUGH, WHICH IS PRONE TO CAUSING INTESTINAL TISSUE BLEEDING DURING GRASPING. FURTHERMORE IT WAS STATED IT IS INTESTINAL TISSUE INJURY. THE CLINICIAN BELIEVES THAT THE INJURY MAY ALSO BE RELATED TO THE PATIENT'S ADVANCED AGE AND FRAGILE INTESTINAL TISSUE, BUT THIS CANNOT BE CONFIRMED. MOREOVER, RC INSPECTION REVEALED THAT THE DEVICE SURFACE WAS NOT SIGNIFICANTLY ROUGH. THE SURGEON PROMPTLY PERFORMED SUTURING ON THE LACERATED BOWEL TISSUE.

  Patient problems: Laceration(s)

  MAUDE report 25260825 ↗
• InjuryMay 21, 2026Insufficient Device Problem Information

  THE FOLLOWING WAS REPORTED: "DURING A LAPAROSCOPIC GASTROINTESTINAL SURGERY, WHILE USING 33310CC, THE DOCTOR TORE THE GASTROINTESTINAL TRACT AND CAUSED BLEEDING WHEN GRASPING INTESTINAL TISSUE."

  Patient problems: Laceration(s)

  MAUDE report 25250249 ↗
• InjuryMay 21, 2026Insufficient Device Problem Information

  THE FOLLOWING WAS REPORTED: "DURING A LAPAROSCOPIC GASTROINTESTINAL SURGERY, WHILE USING 33310CC, THE DOCTOR TORE THE GASTROINTESTINAL TRACT AND CAUSED BLEEDING WHEN GRASPING INTESTINAL TISSUE."

  Patient problems: Laceration(s)

  MAUDE report 25250246 ↗
• MalfunctionMay 28, 2025Material Separation; Detachment of Device or Device Component; Material Separation; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING THE SURGICAL PROCEDURE, THE CURVED FENESTRATED CLAMP PRESENTED A PROBLEM, WHERE THE INTERNAL STEM CAME LOOSE FROM THE TUBE AFTER INSERTION INTO THE ABDOMINAL CAVITY. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22099012 ↗
• MalfunctionNov 4, 2024Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE TIP OF A LAPAROSCOPIC INSTRUMENT INSERT DROPPED DURING USE IN A LIVE PATIENT CASE. BROKEN TIP WAS IMMEDIATELY RECOVERED AND REMOVED FROM THE CAVITY; FAULTY INSTRUMENT WAS PUT ASIDE AND REPLACED WITH ANOTHER LAPAROSCOPIC INSTRUMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20599439 ↗