Medline Industries, Inc. DYNJ17333GRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942286430), received between Feb 21, 2018 and Feb 21, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Contamination of Device Ingredient or Reagent” (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.

• InjuryFeb 21, 2018Contamination of Device Ingredient or Reagent

  IT WAS REPORTED THAT DURING A LAMINECTOMY PROCEDURE THE SURGEON NOTICED THE OPERATING ROOM (OR) TOWEL SHEDDING LINT INTO THE SURGICAL SITE WHICH REQUIRED IRRIGATION TO REMOVE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7286483 ↗