Alaris 30862-0500Recalls & reported problems
BD Switzerland Sàrl · Extension Set, Microbore Tubing, Anti-siphon Valve (Detachable) 157.5 cm (62 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 10885403235221), received between Jul 6, 2020 and Dec 4, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Labelling, Instructions for Use or Training 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
- Labelling, Instructions for Use or Training Problem1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 4, 2025Labelling, Instructions for Use or Training Problem; Labelling, Instructions for Use or Training Problem
IT WAS REPORTED THAT THE BD ALARIS EXTENSION SET W/ ANTISIPHON VALVE HAD INCORRECT LABEL CONTENT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: FOR #30862-0500 THE ONLINE LABEL SAYS A PV OF .6 AND THE LABEL THE CUSTOMER RECEIVED SAY PV 1ML. COULD YOU ADVISE THE REASON FOR THE DIFFERENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23713013 ↗MalfunctionJul 6, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE EXT W/ANTISIPHON VLV LEAKED FROM THE GREEN BD TEXIUM ADAPTOR DURING A "46 HOUR AMBULATORY INFUSION". THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "PT WAS SENT HOME WITH CADD INFUSION PUMP FOR 46 HOUR AMBULATORY INFUSION. PT CALLED NEXT MORNING AND INFORMED INFUSION CENTER THAT PUMP WAS LEAKING. PT TOLD TO TURN OFF PUMP AND COME INTO INFUSION CENTER ASAP. WHEN PT ARRIVED, PUMP WAS CONFIRMED TO BE LEAKING FROM GREEN BD TEXIUM ADAPTOR. COMPONENTS INCLUDE 250 ML CADD CASSETTE, CADD TUBING EXTENSION, AND A GREEN BD TEXIUM ADAPTOR."
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10237681 ↗
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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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