Stryker 0240-031-050Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00700621719533), received between Oct 6, 2023 and Oct 6, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “No Display/Image” (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.

• InjuryOct 6, 2023No Display/Image; No Display/Image

  EVENT DESCRIPTION: "PATIENT PRESENTED FOR ROBOTIC-ASSISTED LAPAROSCOPIC DISTAL PANCREATECTOMY AND SPLENECTOMY. DURING INSERTION OF THE INITIAL TROCAR USING THE CAMERA TO VISUALIZE ENTRY, THE STRYKER MONITOR SCREEN WENT BLANK AND VISUALIZATION WAS LOST. SURGEON HALTED ENTRY, BUT WHEN SCREEN IMAGE RETURNED A MOMENT LATER, THE TROCAR WAS NOTED TO HAVE PERFORATED THE COLON. THE CASE WAS CONVERTED TO OPEN TO FACILITATE REPAIR OF 0.5CM LENGTH TRANSVERSE COLOTOMY. THE SURGERY PROGRESSED AS PLANNED WITH NO FURTHER COMPLICATIONS. LOSS OF VISUALIZATION MAY HAVE CONTRIBUTED TO PATIENT INJURY." ADVERSE CONSEQUENCES DETAILS:THE TROCAR WAS NOTED TO HAVE PERFORATED THE COLON. THE CASE WAS CONVERTED TO OPEN TO FACILITATE REPAIR OF 0.5CM LENGTH TRANSVERSE COLOTOMY. THE SURGERY PROGRESSED AS PLANNED WITH NO FURTHER COMPLICATIONS. LOSS OF VISUALIZATION MAY HAVE CONTRIBUTED TO PATIENT INJURY THIS EVENT HAS BEEN REPORTED BY THE FACILITY UNDER MDR REPORT KEY 17756306, REPORT NUMBER MW5145684.

  Patient problems: Internal Organ Perforation

  MAUDE report 17885885 ↗