AESCULAP JM740Recalls & reported problems
Aesculap AG · Bottom, with base perforation, Standard 3/4, outer length: 470 mm, outer width: 274 mm, outer heigth: 90 mm · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04038653394821), received between Mar 11, 2021 and Mar 11, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
Device problems
- Insufficient Device Problem Information2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 11, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THERE WAS AN ISSUE WITH A STERILCONTAINER S BOTTOM 3/4 90MM. ACCORDING TO THE COMPLAINT DESCRIPTION THERE OCCURED A CYCLE FAILURE WITH THE COMPLAINED CONTAINER. THERE WAS NO PATIENT INVOLVEMENT IN THIS CASE ANOTHER CONTAINER WAS USED. IT HAD TO BE TAKEN OUT REPACKED, CHECKED AND THEN PUT BACK IN AGAIN. THERE WAS NO PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED NOR AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4). ASSOCIATED MEDWATCH-REPORTS: 9610612-2020-00622 ((B)(4) + JM340).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11465409 ↗MalfunctionMar 11, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
ASSOCIATED MEDWATCH-REPORTS: 9610612-2020-00621 (400486093 + JM740), 9610612-2020-00622 (400486094 + JM340).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11465391 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.