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Monoject 8939Recalls & reported problems

Cardinal Health, Inc. · Monoject Chemotherapy Container, Slide Lid, Yellow, 18 Gallon · 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 40884521022769), received between Sep 24, 2019 and Sep 24, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Component” (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

  • Defective Component1
  • Detachment of Device or Device Component1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionSep 24, 2019Defective Component; Detachment of Device or Device Component; Defective Component; Detachment of Device or Device Component

    THE CUSTOMER REPORTED THAT WHEN THEY RECEIVED THE CONTAINERS THE LIDS WOULD NOT SLIDE AND WOULD NOT STAY ATTACHED.

    Patient problems: No Patient Involvement

    MAUDE report 9109653 ↗

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