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AESCULAP ER063RRecalls & reported problems

Aesculap AG · SCHUMACHER Biopsy Forceps, straight, 9 1/2", (240 mm) · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04038653154838), received between Mar 10, 2021 and Mar 11, 2021 — classified as 2 injuries.

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

  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Hemorrhage/Blood Loss/Bleeding2
  • Pain2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 11, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ASSOCIATED MEDWATCH-REPORTS: 9610612-2021-00161(400503235 ER063R), 9610612-2021-00180(400503837 ER063R).

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Pain

    MAUDE report 11466205 ↗
  • InjuryMar 10, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ASSOCIATED MEDWATCH-REPORTS: 9610612-2021-00161((B)(6) ER063R); 9610612-2021-00180((B)(6) ER063R).

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Pain

    MAUDE report 11457357 ↗

Other FORCEPS, BIOPSY, GYNECOLOGICAL devices

All FORCEPS, BIOPSY, GYNECOLOGICAL devices →

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