Medline Industries, Inc. DYNJ904781Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942725342), received between Mar 9, 2018 and Feb 10, 2020 — classified as 2 malfunctions.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 10, 2020Break; Device Fell

  IT WAS REPORTED THAT TWO SURGICAL BLADES BROKE AND A PIECE FELL INTO THE SURGICAL SITE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9686568 ↗
• MalfunctionMar 9, 2018Material Frayed

  IT WAS REPORTED THAT DURING A TOTAL HIP PROCEDURE THE GAUZE FRAYED, SHEDDING LINT INTO THE SURGICAL SITE.

  Patient problems: Foreign Body In Patient

  MAUDE report 7327888 ↗