Medline Industries, Inc. DYNJ43631BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489716993), received between Mar 12, 2026 and Mar 12, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination” (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.

• MalfunctionMar 12, 2026Contamination

  ACCORDING TO THE CUSTOMER CONTACT, "THE INCLUDED BULB SYRINGE HAD AN INSECT INSIDE THE STERILE PACKAGING" AND "THE NURSING TEAM DISCOVERED THE INSECT FLOATING IN THE LIQUID WHEN THEY PULLED SALINE INTO THE BULB."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24579780 ↗