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Monoject 8881202355Recalls & reported problems

Cardinal Health, Inc. · Blunt Cannula · Class 1

All models of Monoject (164)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 10884521012509), received between Nov 21, 2019 and Nov 21, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

Device problems

  • Device Contamination with Chemical or Other Material1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionNov 21, 2019Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

    THE CUSTOMER REPORTED THAT THERE WERE LOSE YELLOW PARTICLES FROM THE HOUSING OF THE NEEDLE THAT TRANSFERRED THREADS ONTO THE NEEDLE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9354258 ↗

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Sources and updates

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