AESCULAP MD347Recalls & reported problems
Aesculap, Inc. · PROCESS INDICATOR CARD SCORED · 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 14522281000508), received between Nov 26, 2024 and Nov 26, 2024 — classified as 1 malfunction.
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
- No Apparent Adverse Event1
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.
MalfunctionNov 26, 2024No Apparent Adverse Event; No Apparent Adverse Event
USER FACILITY REPORTED SEVERAL OF THE STERILE INDICATOR TAGS FOR TRAYS THAT GO TO THE OR (OPERATING ROOM) ARE VERY SIMILAR AND EASILY CONFUSED.LEADING TO POTENTIAL USE OF AN UNCLEAN OR NOT STERILE TRAY FOR A STERILE PROCEDURE. USER FACILITY DID NOT PROVIDE ANY SAMPLES, BATCH NUMBERS OR PICTURES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20782397 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.