Medline Industries, Inc. DYNJ60113Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888277799905), received between Dec 10, 2018 and Dec 10, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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.

• MalfunctionDec 10, 2018Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT IRRIGATION WAS REQUIRED TO REMOVE THE LINT PARTICULATE THAT WAS DISCOVERED FLOATING ON THE PATIENT'S LENS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8147723 ↗