Medline Industries, Inc. DYNJ51754BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942668571), received between Nov 8, 2018 and Nov 8, 2018 — classified as 1 malfunction.

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

• MalfunctionNov 8, 2018Material Frayed

  IT WAS REPORTED THAT FRAYING OF THE X-RAY DETECTABLE GAUZE WAS NOTED IN THE MIDDLE OF THE PROCEDURE AND A TISSUE FORCEPS WAS USED TO SUCCESSFULLY RETRIEVE THE FRAYED FIBERS OF THE X-RAY DETECTABLE GAUZE FROM THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8051260 ↗