KSlock 28272UKNRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551265222), received between Apr 14, 2023 and May 16, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 16, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  DURING THE NEUROSURGICAL INTERVENTION OF COLLOID CYST EXCISION BY VENTRICULAR ENDOSCOPY, THE ENDOSCOPE IS HELD BY A METAL ARM FIXED TO THE INTERVENTION TABLE IN ORDER TO FREE THE SURGEON'S HAND. AT THE END OF THE OPERATION, THE CLAMPING JAW USED TO HOLD THE ENDOSCOPE BROKE, CAUSING MOVEMENT OF THE ENDOSCOPE WHICH WAS IN THE PATIENT'S BRAIN, CAUSING BLEEDING FROM THE EPENDYMAL VEINS AND REDUCING VISIBILITY FOR THE END. INTERVENTION.

  Patient problems: Brain Injury

  MAUDE report 16940967 ↗
• InjuryApr 14, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  DURING THE NEUROSURGICAL INTERVENTION OF COLLOID CYST EXCISION BY VENTRICULAR ENDOSCOPY, THE ENDOSCOPE IS HELD BY A METAL ARM FIXED TO THE INTERVENTION TABLE IN ORDER TO FREE THE SURGEON'S HAND. AT THE END OF THE OPERATION, THE CLAMPING JAW USED TO HOLD THE ENDOSCOPE BROKE, CAUSING MOVEMENT OF THE ENDOSCOPE WHICH WAS IN THE PATIENT'S BRAIN, CAUSING BLEEDING FROM THE EPENDYMAL VEINS AND REDUCING VISIBILITY FOR THE END. INTERVENTION.

  Patient problems: Brain Injury

  MAUDE report 16747120 ↗