Skip to content

MEDLINE DYNC2303Recalls & reported problems

Medline Industries, Inc. · TRAY,IRR PISTON SYR, 0.9% STRL SALINE · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196027682), received between Sep 23, 2019 and Sep 23, 2019 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Urinary Tract Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 23, 2019Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED A URINARY TRACT INFECTION (UTI), WAS HOSPITALIZED, AND TREATED WITH ANTIBIOTICS.

    Patient problems: Urinary Tract Infection

    MAUDE report 9103774 ↗

Other SYRINGE, IRRIGATING (NON DENTAL) devices

All SYRINGE, IRRIGATING (NON DENTAL) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.