NA BOP-7Recalls & reported problems
Fehling Instruments GmbH & Co. KG · CERAMO TC HYP.vascular scissors short bl., 25° ang. 180 mm · Class 1
Data updated Oct 16, 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 04058749007237), received between Aug 7, 2025 and Aug 7, 2025 — classified as 1 malfunction.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
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.
MalfunctionAug 7, 2025Material Fragmentation; Material Fragmentation
ON (B)(6) 2025 WE RECEIVED A COMPLAINT THAT THE TIPS OF 3 SCISSORS (REF: BOP-7) WERE BROKEN. THE SCISSORS HAVE BEEN USED FOR MORE THAN A YEAR. THE SCISSORS ARE REUSABLE INSTRUMENTS AND NEED TO BE REPROCESSED AFTER EACH USE. THE TIP OF ONE SCISSORS (REF: BOP-7) SEEMS TO BE BROKEN DURING SURGERY, BUT WE DON'T KNOW, WHICH OF THE 3 SCISSORS IS SUBJECT TO THIS REPORT. WE RECEIVED THE FOLLOWING INFORMATION FROM OUR CUSTOMER: THE SURGEON DISCOVERED THE DAMAGE ON ONE OF THE SCISSORS DURING A CASE WHILE THE INSTRUMENT WAS INSIDE THE PATIENT. SHE INSISTS THAT THE BLADE BROKE INSIDE THE PATIENT. SHE 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 WE KNOW. ON REQUEST, WE RECEIVED THIS ADDITIONAL INFORMATION FROM OUR CUSTOMER: ASSIST STATES THAT THEY HAD BEEN USING THE SCISSORS THROUGHOUT THE CASE. WHEN THE SURGEON USED THEM TO CUT INTO A CORONARY ARTERY, THE SCISSORS LOOKED INTACT GOING INTO THE ARTERIAL LUMEN. WHEN THE SCISSORS WERE WITHDRAWN, THE TIP WAS MISSING. THE ARTERIAL LUMEN WAS FLUSHED SEVERAL TIMES AND THE SURGICAL AREA INSPECTED. AN X-RA
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22735448 ↗
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
- 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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