Medline Industries, Inc. DYNJ87316Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459026041), received between Feb 12, 2025 and Feb 12, 2025 — classified as 1 injury.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• InjuryFeb 12, 2025Break; Break

  ACCORDING TO THE FACILITY ON 1/3 AT THE END OF A ROBOTIC ASSISTED LAPAROSCOPIC, UMBILICAL HERNIA REPAIR WITH MESH PROCEDURE, "THE RAYTECH WAS PLACED IN THE ABDOMEN AND WAS BEING PULLED THROUGH A ROBOTIC TROCAR AT THE END OF THE CASE AND IT CAME APART".

  Patient problems: Insufficient Information

  MAUDE report 21368840 ↗