CLICKLINE 33310VARecalls & reported problems
Karl Storz GmbH & Co. KG · CLICKLINE Forceps Insert · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04048551134726), received between Apr 17, 2025 and Mar 7, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (3 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.
Reports received per month
Most reported problems
Device problems
- Break3
- Detachment of Device or Device Component2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 7, 2026Break
THE FOLLOWING WAS REPORTED: "THE USER REPORTED THAT THE FORCEPS BROKE OFF AFTER MEDICAL PROCEDURE." NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24540815 ↗InjuryJul 10, 2025Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT AFTER A SURGICAL PROCEDURE, THE HOSPITAL DISCOVERED THAT A RIVET / SCREW WAS MISSING FROM THE FORCEPS. A POST-OPERATIVE CT SCAN DETECTED A FOREIGN BODY WITHIN THE PATIENT. THE HOSPITAL WAS UNABLE TO DETERMINE WHETHER THE FOREIGN BODY SEEN IN THE CT SCAN IS THE MISSING RIVET / SCREW OR NOT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22473340 ↗MalfunctionApr 17, 2025Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT "DEFECT". NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Insufficient Information
MAUDE report 21862317 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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