KSlock 28272HCRecalls & reported problems
Karl Storz GmbH & Co. KG · Articulated Stand, L-shaped, long · 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 04048551111048), received between Jan 27, 2025 and Jan 27, 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
- Insufficient Information1
- 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.
MalfunctionJan 27, 2025Break; Break
IT WAS REPORTED THAT EQUIPMENT BROKE THE SECOND TIME IT WAS USED. THE BROKEN PIECES ALMOST FELL INSIDE THE PATIENT DURING THE PROCEDURE. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 21242214 ↗
Other Endoscope holder devices
- KSlock 28272UKNKarl Storz GmbH & Co. KG · Endoscope holder2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.