CLICKLINE 33310HMRecalls & 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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551134283), received between Jul 26, 2024 and Jul 26, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- 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.
InjuryJul 26, 2024Break; Break
IT WAS REPORTED THAT A SMALL PIN FROM THE INSIDE OF THE DEVICE CAME OFF AND WAS LOST IN THE ABDOMEN WHEN THE INSTRUMENT WAS USED DURING A PROCEDURE. XRAY WERE CALLED TO HELP TO LOCATE THE PIN. THE PIN WAS LOCATED AND SUCCESSFULLY RETRIEVED. THE INSTRUMENT WAS IN WORKING ORDER PRIOR TO THIS. IT WAS CHECKED BY THE SCRUB NURSE AND USED BY THE SURGEON BEFORE THE PIN CAME LOOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19837529 ↗InjuryJul 26, 2024Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT A SMALL PIN FROM THE INSIDE OF THE DEVICE CAME OFF AND WAS LOST IN THE ABDOMEN WHEN THE INSTRUMENT WAS USED DURING A PROCEDURE. XRAY WERE CALLED TO HELP TO LOCATE THE PIN. THE PIN WAS LOCATED AND SUCCESSFULLY RETRIEVED. THE INSTRUMENT WAS IN WORKING ORDER PRIOR TO THIS. IT WAS CHECKED BY THE SCRUB NURSE AND USED BY THE SURGEON BEFORE THE PIN CAME LOOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19837304 ↗
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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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