CLICKLINE 33410LFRecalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551143087), received between Nov 3, 2023 and Dec 23, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Chemical Problem1
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 23, 2025Break; Chemical Problem; Break; Chemical Problem
IT WAS REPORTED THAT THE DEVICE IS BROKEN/JAMMED. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE MDR: 9610617-2025-02420.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23879084 ↗MalfunctionNov 3, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT ONE SIDE OF THE LAPAROSCOPIC FLAT BOWEL GRASPER BROKE OFF WHILE INSIDE OF THE PATIENT, BUT ALL PARTS WERE REMOVED FROM PATIENT. NO INJURY TO THE PATIENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18070084 ↗
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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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