n.a. 27040XALRecalls & reported problems
Karl Storz GmbH & Co. KG · Inner Tube for 27040 SD/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 04048551076545), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Display or Visual Feedback 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.
Reports received per month
Most reported problems
Device problems
- Display or Visual Feedback Problem1
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.
MalfunctionOct 15, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem
IT WAS REPORTED THAT "COMBINATION OF 27040XAL AND 27068CD BRIDGE CAUSED POOR IMAGE ON SCREEN". IT WAS CONFIRMED THAT THERE WAS NO PATIENT INJURY OR IMPACT DUE TO THE REPORTED ISSUE AND THE SURGEON WAS ABLE TO COMPLETE THE PROCEDURE WITHOUT DELAY. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED. CROSS REFERENCE COMPLAINT ID (ON THE 27068CD BRIDGE AS A COCONMITANT ITEM): (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23281755 ↗
Other CYSTOURETHROSCOPE devices
- n.a. 11272C1Karl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall16 reports
- n.a. 11272VNUKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall4 reports
- n.a. 27050CAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE54 reports
- C-VIEW 11272VKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- n.a. 11272VNKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VUAKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
- C-VIEW 11272VUKarl Storz GmbH & Co. KG · CYSTOURETHROSCOPE1 recall0 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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