Alaris C25006Recalls & reported problems
BD Switzerland Sàrl · Extension Set, Microbore Tubing 213 cm (84 in) · Class 2
All models of Alaris (85)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10885403235603), received between Aug 13, 2020 and Aug 1, 2023 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (4 reports).
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
- Complete Blockage4
- Obstruction of Flow1
- Restricted Flow rate1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 1, 2023Complete Blockage; Complete Blockage
IT WAS REPORTED THAT BD ALARIS EXTENSION SET WAS OCCLUDED. THE FOLLOWING WAS RECIEVED BYT THE INITITAL REPORTER: VERBATIM: CUSTOMER REPORTED THAT THIS ALARIS MICROBORE TUBING IS UNABLE TO BE FLUSHED AND UPON EXAMINATION, IT'S NOTED THAT THE HUB IS NEARLY 100% OCCLUDED WITH PLASTIC, PREVENTING ANY FLUID FROM BEING ADMINISTERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17435730 ↗MalfunctionSep 30, 2022Complete Blockage; Complete Blockage
IT WAS REPORTED WHILE USING BD ALARIS EXTENSION SET 84 INCH EXT SET THE TUBING WAS CLOGGED. THIS OCCURRED 5 TIMES. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONCERN DESCRIPTION: UNBABLE TO FLUSH/PRIME TUBING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15516165 ↗MalfunctionSep 30, 2022Complete Blockage; Complete Blockage
IT WAS REPORTED WHILE USING BD ALARIS EXTENSION SET 84 INCH EXT SET THE TUBING WAS CLOGGED. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONCERN DESCRIPTION: UNBABLE TO FLUSH/PRIME TUBING
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15516043 ↗MalfunctionJan 10, 2022Obstruction of Flow; Obstruction of Flow
IT WAS REPORTED THAT THE BD ALARIS¿ EXTENSION SET WAS UNABLE TO PRIME. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY CUSTOMER THAT WHERE THE BD EXTENSION SET (MICROBORE TUBING) WOULD NOT PRIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13206349 ↗MalfunctionAug 13, 2020Complete Blockage; Restricted Flow rate; Complete Blockage; Restricted Flow rate
IT WAS REPORTED THAT THE BOX OF 84 INCH EXT SET TUBING UNITS WOULD NOT PUSH PROPOFOL THROUGH THEM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT WAS ONLY REPORTED TO ME THAT THE TUBING WILL NOT WORK AS AN EXTENSION SET IN OUR COVID UNIT.. AND NOT TO BRING ANY MORE. I DO KNOW FOR SURE, THEY WERE UNABLE TO PUSH THE DRUG PROPOFOL, BUT WHEN WE USED OTHER TUBING FROM BD, AS AN EXTENSION, WE COULD.". "THE MICRO TUBING WILL NOT PUSH THE THICKER DRUGS THROUGH IT".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10402782 ↗
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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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