Alaris 25203Recalls & reported problems
BD Switzerland Sàrl · Extension Set, 3-Way Stopcock, Lipid Resistant 51 cm (20 in) · Class 2
All models of Alaris (85)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10885403233272), received between Jan 17, 2024 and Jan 17, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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.
Reports received per month
Most reported problems
Device problems
- Infusion or Flow Problem1
- Material Separation1
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 17, 2024Material Separation; Material Separation
IT WAS REPORTED THAT BD ALARIS EXTENSION SET WAS SEPARATED THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM "BD NUMBER 25203 IS KINKING FOR THE PEDIATRIC PATIENTS""THEY DEFINITELY COME APART TOO EASILY. WHICH IS A HUGE RISK IN OUR AREA."
Patient problems: Insufficient Information
MAUDE report 18528443 ↗MalfunctionJan 17, 2024Infusion or Flow Problem; Infusion or Flow Problem
IT WAS REPORTED THAT BD ALARIS EXTENSION SET WAS KINKED THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE VERBATIM. "BD NUMBER 25203 IS KINKING FOR THE PEDIATRIC PATIENTS""THEY DEFINITELY COME APART TOO EASILY. WHICH IS A HUGE RISK IN OUR AREA."
Patient problems: Insufficient Information
MAUDE report 18528437 ↗
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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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