Snowden-Pencer 89-5100BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403278617), received between Oct 20, 2020 and Oct 20, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 20, 2020Material Separation; Material Separation

  IT WAS REPORTED THAT THE SCISSOR TIP DISENGAGED FROM THE HANDLE AND FELL INTO THE PATIENT DURING A PROCEDURE CAUSING THE SURGEON TO HAVE TO OPEN UP THE PATIENT. IT WAS DURING A LAP CHOLE PROCEDURE. THE TIP WAS RETRIEVED LAPAROSCOPICALLY DURING A FLUOROSCOPY. THE PATIENT WAS REPORTED TO BE STABLE BUT THERE WAS A DELAY TO THE PROCEDURE. THE PROCEDURE WAS COMPLETED AS PLANNED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10705636 ↗