CLICKLINE 33510DURecalls & reported problems
Karl Storz GmbH & Co. KG · CLICKLINE Forceps Insert · Class 2
All models of CLICKLINE (46)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551151044), received between Jan 23, 2025 and Jan 23, 2025 — classified as 1 malfunction.
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. 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
- Break1
- Detachment of Device or Device Component1
- Device Dislodged or Dislocated1
- Material Separation1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2025Break; Material Separation; Detachment of Device or Device Component; Device Dislodged or Dislocated; Break; Material Separation; Detachment of Device or Device Component; Device Dislodged or Dislocated
IT WAS REPORTED THAT: "THE FORCEPS WAS INSERTED INTO THE PATIENT'S ABDOMINAL CAVITY. WHEN THE FORCEPS WAS OPENED, A GROOVE CAME LOOSE FROM THE INLAY AND FELL INTO THE PATIENT. SINCE THE GROOVE COULD BE REMOVED FROM THE PATIENT IMMEDIATELY, THERE WAS NO SIGNIFICANT DELAY REPORTED. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Insufficient Information
MAUDE report 21219235 ↗
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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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