AESCULAP MB207RRecalls & reported problems
Aesculap, Inc. · METZENBAUM DUROTIP TC Dissecting Scissors, curved, 5 3/4", (145 mm), delicate pattern, sharp/sharp · 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 04046964683688), received between Nov 17, 2023 and Nov 17, 2023 — 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.
Reports received per month
Most reported problems
Device problems
- Break1
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 17, 2023Break; Break
IT WAS REPORTED TO AESCULAP INC. THAT A TC METZENBAUM SCISS DEL CVD S/S 145MM (PART # MB207R) WAS USED DURING A PROCEDURE ON (B)(6) 2023. ACCORDING TO THE COMPLAINANT THE TIP OF THE DEVICE HAD BROKEN OFF DURING USE. REPORTEDLY THE TIP WAS RETRIEVED AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A DIFFERENT INSTRUMENT. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. THE ADVERSE EVENT IS FILED UNDER AIC REFERENCE (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18162934 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.