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ChemoPlus CP3005ARecalls & reported problems

Cardinal Health, Inc. · Silver IVA Seals · Class 2

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 10884527005857), received between Sep 20, 2017 and Sep 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Problem with Sterilization” (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

  • Problem with Sterilization1

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 20, 2017Problem with Sterilization; Problem with Sterilization

    THE CUSTOMER STATES THAT THE PRODUCT STICKS TO THE SIDE OF THE BAG OR THE SYRINGE AND THE FOIL ON TOP IT TEARS OR ITS HARD TO REMOVE.

    Patient problems: No Patient Involvement

    MAUDE report 6880234 ↗

Other CONTAINER, I.V. devices

All CONTAINER, I.V. devices →

Sources and updates

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