MEDLINE INDUSTRIES, INC. DYNJ33650ORecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459480973), received between Jan 8, 2026 and Jan 8, 2026 — classified as 1 malfunction.

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.

• MalfunctionJan 8, 2026

  DURING SETUP OF THE STERILE BACK TABLE, A SHORT BROWN HAIR WAS DISCOVERED ON THE STERILE LIGHT HANDLE CONTAINED IN THE LOWER EXTREMITY PACK. AS A RESULT, THE ENTIRE BACK TABLE WAS DEEMED CONTAMINATED. ALL SUPPLIES WERE DISCARDED OR REPLACED, AND ALL INSTRUMENTS REQUIRED DECONTAMINATION AND RE-STERILIZATION, CAUSING A DELAY IN THE PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24002583 ↗