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AESCULAP US345Recalls & reported problems

Aesculap, Inc. · Forceps, 6", (153 mm), width: 0,70 mm · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

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 04046964582509), received between Jul 20, 2022 and Jul 20, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 20, 2022Break; Insufficient Device Problem Information; Break; Insufficient Device Problem Information

    IT WAS REPORTED TO AESCULAP INC. THAT A BIPOLAR FCPS RNDMICROSTR .7MM153MM (PART # US345) WAS USED DURING A PROCEDURE PERFORMED ON (B)(6) 2022. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE FORCEPS WERE STICKING WHILE CAUTERIZING, WHICH LED TO VESSEL DAMAGE. THE COMPLAINT DEVICE WAS RETURNED TO THE MANUFACTURER FOR EVALUATION. ALTHOUGH REQUESTED, NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE.

    Patient problems: Insufficient Information

    MAUDE report 15067075 ↗

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Sources and updates

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