AESCULAP BC061RRecalls & reported problems
Aesculap AG · Delicate Scissors, curved, 4 1/4", (110 mm), delicate pattern, sharp/sharp, non-sterile, reusable · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 04038653020324), received between Aug 19, 2022 and Aug 19, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Fragmentation” (2 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Material Fragmentation2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 19, 2022Material Fragmentation; Material Fragmentation
IT WAS REPORTED TO AESCULAP INC. THAT IRIS SCISSORS CVD.S/S 110MM (PART # BC061R) WERE USED DURING A PROCEDURE PERFORMED ON (B)(6) 2022. ACCORDING TO THE COMPLAINANT, THE CURVED IRIS SCISSORS BROKE IN THE PATIENT'S NOSE WHILE SURGEON WAS PERFORMING NASAL SURGERY. THE COMPLAINT DEVICE HAS NOT BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION. AN ADDITIONAL MEDICAL INTERVENTION WAS NECESSARY. ALTHOUGH REQUESTED, ADDITIONAL INFORMATION HAS NOT BEEN MADE AVAILABLE. THE ADVERSE EVENT IS FILED UNDER AIC REFERENCE (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15260727 ↗InjuryAug 19, 2022Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT THERE WAS AN ISSUE WITH IRIS SCISSORS CVD.S/S 110MM - BC061R. ACCORDING TO THE COMPLAINT DESCRIPTION, THE CURVED IRUS SCISSORS BROKE IN THE PATIENT'S NOSE WHILE SURGEON WAS PERFORMING NASAL SURGERY. AN ADDITIONAL MEDICAL INTERVENTION WAS NECESSARY. ADDITIONAL INFORMATION WAS NOT PROVIDED. ADDITIONAL PATIENT INFORMATION IS NOT AVAILABLE. THE ADVERSE EVENT IS FILED UNDER AAG REFERENCE (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15260687 ↗
Other SCISSORS, GENERAL, SURGICAL devices
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- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Sklar Instruments 96-2673ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2266Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2502Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion TRI67630Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2492ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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