NA BSI-6SRecalls & reported problems
Fehling Instruments GmbH & Co. KG · CERAMO-S RONDO micro vessel scissors, angl. 45°, 210 mm · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04058749009590), received between Mar 19, 2026 and Mar 19, 2026 — classified as 1 malfunction.
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.
MalfunctionMar 19, 2026Break
BROKEN TIP: ITEM RETURNED TO THE OR FROM AEMP WITH A BROKEN TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24637425 ↗
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- Needle NDL-107-04Galt Medical Corp. · Instruments, Surgical, Cardiovascular1 recall0 reports
- ADVANTA SLIDER GDS 22092Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.