Medline Industries, Inc. DYNJ59172BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489237580), received between Nov 25, 2020 and Nov 25, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

• InjuryNov 25, 2020Device Dislodged or Dislocated

  IT WAS REPORTED VIA MEDWATCH REPORT (MW5096598) THAT DURING A PROCEDURE DISLODGEMENT OF A CANNULA FROM A SYRINGE THAT IT ENTERED THE RIGHT EYE OF A PATIENT AND CAUSED AN INJURY.

  Patient problems: Retinal Detachment

  MAUDE report 10906998 ↗