n.a. 27050CBRecalls & reported problems
Karl Storz GmbH & Co. KG · Inner Sheath for 27050 SD · 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 04048551007471), received between Dec 11, 2025 and Dec 11, 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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 11, 2025Break; Break
IT WAS REPORTED THAT "THAT THE CERAMIC BEAK BROKE OFF IN THE PATIENT'S BLADDER DURING A PROCEDURE". NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23785068 ↗
Other CYSTOURETHROSCOPE devices
- n.a. 11272C1Karl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall16 reports
- n.a. 27050CAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE54 reports
- n.a. 11272VNUKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall4 reports
- C-VIEW 11272VUKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- n.a. 11272CU1Karl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VUAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.