MEDLINE INDUSTRIES, INC. DYNJ32228LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459369186), received between Mar 12, 2026 and Mar 12, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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, 2026Defective Device

  CUSTOMER CONTACT REPORTED THAT ON (B)(6) 2026 THERE WAS A "DEFECTIVE SYRINGE." AS A RESULT OF THE INCIDENT, THE CUSTOMER REPORTED "THEY PULLED A SINGLE STERILE ITEM OFF THE SHELF." PER CUSTOMER CONTACT, THE INDIVIDUAL/USER IS DOING "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24584150 ↗