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n.a. 26055XBRecalls & reported problems

Karl Storz GmbH & Co. KG · Inner Sheath, fixed, for 26055 SL · Class 2

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 04048551275573), received between Dec 11, 2020 and Dec 11, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (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.

Most reported problems

Device problems

  • Material Integrity Problem1

Patient problems

  • Foreign Body In Patient1
  • Patient Problem/Medical Problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 11, 2020Material Integrity Problem; Material Integrity Problem

    THE CERAMIC BEAK OF A SHEATH BROKE OFF WHILE INSIDE A PATIENT. TWO BROKEN PIECES WERE RETRIEVED FROM PATIENT. SECOND INSTRUMENT USED FOR OBSERVATION, NO REMAINING PIECES FOUND. NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: Foreign Body In Patient; Patient Problem/Medical Problem

    MAUDE report 10993483 ↗

Other HYSTEROSCOPE (AND ACCESSORIES) devices

All HYSTEROSCOPE (AND ACCESSORIES) devices →

Sources and updates

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