n.a. 27770DRecalls & reported problems
Karl Storz GmbH & Co. KG · Coagulating Electrode, 7 Fr. · Class 2
- 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 04048551089972), received between Dec 23, 2025 and Dec 23, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 23, 2025Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT WHILE THE DOCTOR WAS USING THE ITEM, THE ELECTRODE HEAD FELL OFF IN THE PATIENT'S BLADDER. THE DOCTOR WAS ABLE TO RETRIEVE THE ELECTRODE WITH NO DAMAGE TO THE PATIENT. 2-3 MINUTE DELAY IN THE PROCEDURE. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23877454 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.