AESCULAP US109Recalls & reported problems
Aesculap, Inc. · ADSON TC Tissue Forceps, 4 3/4", (120 mm), toothed (1x2), non-sterile, reusable · 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 04046955076949), received between Oct 23, 2020 and Oct 23, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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 Fragmentation1
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.
InjuryOct 23, 2020Material Fragmentation; Material Fragmentation
ADDITIONAL INFORMATION WAS RECEIVED VIA RECEIPT OF MW 5097029: THE TEETH PORTION ON THE ADSON FORCEPS SEPARATED AND CAME OFF; THIS OCCURRED WHEN MAKING THE INITIAL INCISION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10726678 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.