CLICKLINE 33310KRecalls & reported problems
Karl Storz GmbH & Co. KG · Forceps Insert · Class 2
All models of CLICKLINE (46)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04048551134290), received between Apr 4, 2025 and Dec 23, 2025 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Sharp Edges” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Sharp Edges2
- Mechanical Problem1
Patient problems
- Liver Laceration(s)2
- Gastrointestinal Hemorrhage1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryDec 23, 2025Sharp Edges; Sharp Edges
IT HAS BEEN REPORTED THE SURGEON HAD A SITUATION WHERE THE CUL-DE-SAC HAD A SIGNIFICANT AMOUNT OF BLOOD IN IT AND BLINDLY GRASPED THE BOWEL INSTEAD OF THE CYST THEY INTENDED TO RETRIEVE. THE SURGEON WAS SPECULATIVE THAT THE SHARP EDGE COULD HAVE CUT THE SEROSA. SINCE THE PATIENT GOT INJURED, THE CASE IS DEEMED AS REPORTABLE.
Patient problems: Liver Laceration(s)
MAUDE report 23879087 ↗MalfunctionDec 23, 2025Sharp Edges; Sharp Edges
IT HAS BEEN REPORTED THE SURGEON HAD A SITUATION WHERE THE CUL-DE-SAC HAD A SIGNIFICANT AMOUNT OF BLOOD IN IT AND BLINDLY GRASPED THE BOWEL INSTEAD OF THE CYST THEY INTENDED TO RETRIEVE. THE SURGEON WAS SPECULATIVE THAT THE SHARP EDGE COULD HAVE CUT THE SEROSA. SINCE THE PATIENT GOT INJURED, THE CASE IS DEEMED AS REPORTABLE.
Patient problems: Liver Laceration(s)
MAUDE report 23879085 ↗InjuryApr 4, 2025Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THE SURGEON HAD A SITUATION WHERE THE GRASPER GOT STUCK IN THE OMENTUM AND IT TOOK SOME GENTLE DISSECTION TO GET IT OUT. THE SHARP CORNER WHERE THE GRASPER IS CONNECTS TO THE SHAFT IS WHAT WAS STUCK. THE SURGEON HAD A SITUATION WHERE THE GRASPER GOT STUCK IN THE OMENTUM AND IT TOOK SOME GENTLE DISSECTION TO GET IT OUT. THE SHARP CORNER WHERE THE GRASPER IS CONNECTS TO THE SHAFT IS WHAT WAS STUCK. SMALL EPIPLOICA SEROSAL INJURY AS IT WAS SNAGGED ON THE EPIPLOICA - HOWEVER, IF THIS HAPPENED ON THE BOWEL SEROSA, IT COULD CAUSE A PERFORATION/TEAR OF THE BOWEL, EXPECTANTLY MANAGED. DUE TO THE SMALL EPIPLOICA.
Patient problems: Gastrointestinal Hemorrhage
MAUDE report 21778479 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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