n.a. 11302BD2Recalls & reported problems
Karl Storz GmbH & Co. KG · Intubation Fiberscope 3.7 x 65 · Class 1
- 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 04048551226810), received between Jul 10, 2025 and Jul 10, 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
- Failure to Disconnect1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2025Break; Failure to Disconnect; Break; Failure to Disconnect
IT WAS REPORTED THAT THE SUCTION CONNECTOR HAS BEEN BROKEN DURING BRONCHOSCOPY (BROKEN AT THE BASE WHERE IT ATTACHES TO THE BRONCHOSCOPE), CAUSING COMPLETELY THE SPRING INSIDE TO DETACH. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Insufficient Information
MAUDE report 22474879 ↗
Other LARYNGOSCOPE, NON-RIGID devices
- n.a. 091361-06Karl Storz GmbH & Co. KG · LARYNGOSCOPE, NON-RIGID10 reports
- C-MAC 11301BNXKarl Storz GmbH & Co. KG · LARYNGOSCOPE, NON-RIGID2 reports
- n.a. 11301BN1Karl Storz GmbH & Co. KG · LARYNGOSCOPE, NON-RIGID2 reports
- n.a. 11303BNXKarl Storz GmbH & Co. KG · LARYNGOSCOPE, NON-RIGID2 reports
- NA 091361-01Karl Storz GmbH & Co. KG · LARYNGOSCOPE, NON-RIGID2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.