Alaris, SmartSite C24104ERecalls & reported problems
BD Switzerland Sàrl · Pump Infusion Set, Back Check Valve, 4-Way Stopcock, 3 Y-Sites 386 cm (152 in) Extension Set, with Connector 22 cm (9 in) · Class 2
All models of Alaris, SmartSite (160)
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 10885403235535), received between Feb 6, 2019 and Feb 6, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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
- Fluid/Blood Leak1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 6, 2019Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT DURING AN INFUSION OF NACL, THE TUBING LEAKED AT THE HUB CONNECTION CLOSEST TO THE PATIENT. THERE WAS NO REPORT OF PATIENT HARM. ALTHOUGH REQUESTED, NO OTHER INFORMATION HAS BEEN RECEIVED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8313670 ↗
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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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