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AESCULAP JN744Recalls & reported problems

Aesculap AG · Bottom, with base perforation, outer length: 470 mm, outer width: 274 mm, outer heigth: 187 mm · 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 04046963449377), received between Sep 17, 2021 and Sep 17, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Residue After Decontamination” (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

  • Residue After Decontamination1

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.

  • MalfunctionSep 17, 2021Residue After Decontamination; Residue After Decontamination

    IT WAS REPORTED THAT THERE WAS AN ISSUE WITH JN744: BOTTOM F/CONT. 3/4 PERFORAT. HEIGHT: 187MM. ACCORDING TO THE COMPLAINT DESCRIPTION, RESIDUES WERE FOUND ON CONTAINERS. SMALL RUST COLORED AND RED DOTS OR MARKS APPEAR IN THE CONTAINER. 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 12488770 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.