Alaris 10010985Recalls & reported problems
BD Switzerland Sàrl · Secondary Blood Set, 200 Micron Filter, Nonvented 83 cm (33 in) · Class 2
- 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 10885403233586), received between Nov 6, 2020 and Nov 6, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper Flow or Infusion” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Improper Flow or Infusion1
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.
MalfunctionNov 6, 2020Improper Flow or Infusion; Improper Flow or Infusion
IT WAS REPORTED THAT BLD SET 200MF 20DP 1SPK HAD BLOOD RUN THROUGH IT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL #: 2426-0007; BATCH #: 20085891. IT WAS REPORTED THAT THE TUBING WAS BACKED UP TO THE MAIN IV AND THE NURSE RAN BLOOD THROUGH THE IV PUMP. VERBATIM: THIS IS THE TUBING THAT BACKED UP TO THE MAIN IV . UNABLE TO SEQUESTER THE TUBING SINCE IT WAS DISCARDED BY THE NURSE . PER THE NIGHT SHIFT THEY WERE RUNNING THE BLOOD THROUGH THE IV PUMP.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10804959 ↗
Other Set, administration, intravascular devices
- Autosoft XC 1001680Unomedical A/S · Set, Administration, Intravascular1 death16,105 reports
- Autosoft90™ 1002817Unomedical A/S · Set, Administration, Intravascular1 recall11,907 reports
- Minimed™ Quick-set™ MMT-399AUnomedical A/S · Set, Administration, Intravascular9 deaths8,669 reports
- Medtronic Extended MMT-431AUnomedical A/S · Set, Administration, Intravascular3 deaths8,574 reports
- MiniMed™ Mio™ Advance MMT-242AUnomedical A/S · Set, Administration, Intravascular15 deaths8,164 reports
- CADD 21-7302-24Icu Medical, Inc. · Set, administration, intravascular4 recalls1 death4,657 reports
- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
- Minimed™ Quick-set™ MMT-397AUnomedical A/S · Set, Administration, Intravascular19 deaths4,134 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.