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AESCULAP ER064RRecalls & reported problems

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653154845), received between Nov 6, 2021 and Nov 6, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Material Separation” (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

  • Material Separation1

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.

  • InjuryNov 6, 2021Material Separation; Material Separation

    CORRECTION/ADDITIONAL INFORMATION: PATIENT HARM CHANGED TO ADDITIONAL MEDICAL INTERVENTION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12755836 ↗

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.