n.a. 27770CRecalls & reported problems
Karl Storz GmbH & Co. KG · Coagulating Electrode, 6 Fr. · Class 2
- 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 04048551089965), received between Dec 2, 2024 and Dec 2, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 2, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING PROCEDURE, TIP NOTICED MISSING UPON WITHDRAWAL. UNABLE TO FIND TIP. SURGEON ASSESSED RISK TO PATIENT AS VERY LOW EVEN IF IT WAS STILL IN THE BLADDER. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 20824980 ↗InjuryDec 2, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING PROCEDURE, TIP NOTICED MISSING UPON WITHDRAWAL. UNABLE TO FIND TIP. SURGEON ASSESSED RISK TO PATIENT AS VERY LOW EVEN IF IT WAS STILL IN THE BLADDER. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 20820479 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.