Alaris C24117Recalls & reported problems
BD Switzerland Sàrl · Pump Infusion Set, Low Sorbing Tubing (PE Lined) 286 cm (113 in) · Class 2
All models of Alaris (85)
Data updated Oct 16, 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 10885403232374), received between Mar 25, 2021 and Mar 25, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Free or Unrestricted Flow” (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 16, 2026.
Most reported problems
Device problems
- Free or Unrestricted Flow1
Patient problems
- Hypersensitivity/Allergic reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 25, 2021Free or Unrestricted Flow; Free or Unrestricted Flow
IT WAS REPORTED THAT THE AS LVP 20D LOW SORB HAD FLOW ISSUES DUE TO MEDICATION RUNNING DOWN THE TUBING DURING THE PRIMING PROCESS AND CAUSING HYPERSENSITIVITY IN THE PATIENT. THIS COMPLAINT WAS CREATED TO CAPTURE THE 2ND OF 3 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE REASON I AM ASKING FOR THIS INFORMATION IS THAT NURSES HAVE REPORTED EPISODES THAT PATIENTS HAVING A HYPERSENSITIVITY REACTION TO DRUGS THAT ARE BEING RUN DOWN DURING PRIMING OF THE TUBING, BUT BASED ON THEIR PRIMING VOLUME, IT SHOULD NOT HAVE REACHED THE PATIENT YET. I KNOW THE PACKAGING STATES TO FILL 2/3S OF THE CHAMBER WITH FLUID."
Patient problems: Hypersensitivity/Allergic reaction
MAUDE report 11572459 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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