ChemoPlus CP3009RRecalls & reported problems
Cardinal Health, Inc. · Red 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 10884527006182), received between Jul 21, 2021 and Jul 21, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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
- Material Separation1
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.
MalfunctionJul 21, 2021Material Separation; Material Separation
THE CUSTOMER REPORTED THE MATERIAL OF THE IVA SEAL 36 MM FOIL SEALS FOR THE CEFUROXIME DOSE VIALS CAPS HAS DETERIORATED. THE FOILS CANNOT BE REMOVED FROM THE TOP OF THE CAP IN ONE PIECE, AS THE STRIPPING STRIP REMAINS IN THE HAND AFTER WHICH IT IS DIFFICULT TO GET THE FINAL FOIL OFF THE CAP. THERE HAS BEEN NO PROBLEM WITH THAT FOIL IN THE PAST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12206133 ↗
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- APEX™ 2112530B. Braun Medical Inc. · CONTAINER, I.V.66 reports
- INTRAVIA 2B8013Baxter International Inc. · CONTAINER, I.V.64 reports
- MICROTEK 1Microtek Medical LLC · CONTAINER, I.V.1 recall8 reports
- SECURE® 66040Metrix Company, The · Container, I.V.1 recall8 reports
- SECURE® 66045Metrix Company, The · Container, I.V.1 recall7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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