Medline Industries, Inc. DYNJ50948Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942106028), received between Oct 30, 2018 and Oct 30, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• MalfunctionOct 30, 2018Detachment of Device or Device Component; Device Fell

  IT WAS REPORTED THAT DURING AN UNIDENTIFIED OPHTHALMIC PROCEDURE, FIBERS FROM AN UNIDENTIFIED COMPONENT WERE FOUND TO HAVE FALLEN INTO THE PATIENT'S EYE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8019476 ↗