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Monoject 8881516937Recalls & reported problems

Cardinal Health, Inc. · 6 mL Syringe Luer-Lock Tip · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521014190), received between Apr 12, 2022 and Apr 12, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Physical Resistance/Sticking1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 12, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

    THE CUSTOMER REPORTED THAT THEY DRAW THE FLUID INTO THE SYRINGE AND WHEN INJECTING THE FLUID INTO THE PATIENT, THE SYRINGE STOPS BETWEEN THE 2 AND 1 ML MARKER. PER ADDITIONAL INFORMATION RECEIVED ON 29-MAR-2022, THE PLUNGER WAS STICKING. AFTER SWITCHING THE MEDICATION FROM DEPO-MEDROL TO TRIAMCINOLONE, NO FURTHER ISSUES OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14085244 ↗

Other Syringe, piston devices

All Syringe, piston devices →

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