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Monoject 8935Recalls & reported problems

Cardinal Health, Inc. · Monoject Sharps Container, Slide Lid, Red, 12 Gallon · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 40884521022226), received between Apr 24, 2018 and Feb 28, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Crack” (2 reports).

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

  • Crack2

Patient problems

  • No Known Impact Or Consequence To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 28, 2020Crack; Crack

    THE CUSTOMER REPORTED THAT THERE WERE CRACKS ON THE LID AND BODY OF THE CONTAINER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9772233 ↗
  • MalfunctionApr 24, 2018Crack; Crack

    CUSTOMER REPORTED THAT THE CONTAINER WAS CRACKED.

    Patient problems: No Patient Involvement

    MAUDE report 7456147 ↗

Other Container, sharps devices

All Container, sharps devices →

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