AESCULAP PL541SRecalls & reported problems
Aesculap AG · ATR.INTESTINE.CLIP JAW LENGTH 70MM 3.94N · 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 04046963142476), received between Mar 16, 2021 and Mar 16, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
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.
MalfunctionMar 16, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THERE WAS AN ISSUE WITH PL541S - ATR.INTESTINE.CLIP JAW LENGTH 70MM 3.94N. ACCORDING TO THE COMPLAINT DESCRIPTION, THE CLIP IS MISALIGNED. IN LAPARO GASTRIC SURGERY, AN INTESTINAL CLIP WAS GRASPED IN THE DUODENUM AND THE STOMACH WAS INFLATED WITH AIR UNDER AN ENDOSCOPE. AT THAT TIME, THE CLIP FELL OFF. WHEN CHECKED THE CLIP, THE CLIP WAS MISALIGNED AND HAS A GAP OF ABOUT 2 MM. THERE WAS NO DESCRIBED PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED. ADDITIONAL PATIENT INFORMATION IS NOT AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11495153 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.