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AESCULAP JK388Recalls & reported problems

Aesculap AG · Inner Lid, basis, Standard 1/2, gold, outer length: 298 mm, outer width: 285 mm, outer heigth: 46 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 04038653294060), received between Nov 10, 2021 and Nov 10, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Fell” (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 Fell1

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 10, 2021Device Fell; Device Fell

    IT WAS REPORTED THAT THERE WAS AN ISSUE WITH JK388-1/2-SIZE LID W/RETENTION PLATE GOLD. ACCORDING TO THE COMPLAINT DESCRIPTION, IT WAS REPORTED THAT THE DEVICE FELL. THIS EVENT/MALFUNCTION PROLONGED THE SURGERY FOR 15 MINUTES. ADDITIONAL INFORMATION WAS NOT PROVIDED NOR AVAILABLE / WAS NOT AVAILABLE. THE ADVERSE EVENT / MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12787841 ↗

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