NA BOP-9Recalls & reported problems
Fehling Instruments GmbH & Co. KG · CERAMO TC HYP.vascular scissors, short bl., 125° ang. 170 mm · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 04058749007251), 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
A DISTRIBUTOR INFORMED US THAT A CUSTOMER CLAIMED THAT SOME OF THE DAMAGED SCISSOR BLADES WERE DISCOVERED IN THE OR BUT BEFORE THEY HAD BEEN USED INSIDE THE PATIENT. THE SURGEON DISCOVERED THE DAMAGE ON ONE OF THE SCISSORS (THE DISTRIBUTOR DOESN'T KNOW WHICH ONE) DURING A CASE WHILE THE INSTRUMENT WAS INSIDE THE PATIENT. THE SURGEON INSISTS THAT THE BLADE BROKE INSIDE THE PATIENT. THE SURGEON PAUSED THE SURGERY AND USED A C-ARM X-RAY MACHINE TO SEARCH FOR THE BLADE FRAGMENT IN THE PATIENT, BUT SHE NEVER FOUND THE FRAGMENT AND THE PATIENT IS STILL ALIVE WITH NO COMPLICATIONS AS FAR AS THE DISTRIBUTOR KNOWS. IT IS SUSPECTED THAT ALL THESE INSTRUMENTS WERE DAMAGED DUE TO IMPROPER HANDLING OUTSIDE OF THE OPERATING ROOM, AND IT WAS SIMPLY UNFORTUNATE TIMING THAT THE DAMAGE WAS NOT DISCOVERED BEFORE THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24637218 ↗
Other Scissors, General, Surgical devices
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 reports
- MEDLINE DYND04000Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls0 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Centurion I68790Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66150Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66350Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 67645Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66710Centurion Medical Products 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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