Alaris 10010761Recalls & reported problems
BD Switzerland Sàrl · Pump Infusion Set, Yellow-Striped Microbore Tubing 237 cm (94 in) · Class 2
All models of Alaris (85)
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 07613203021333), received between Nov 22, 2017 and Nov 22, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment Of Device Component” (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
- Detachment Of Device Component1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2017Detachment Of Device Component
IV TUBING PRIMED ADEQUATELY, REMOVED THE TUBING FROM THE ALARIS INFUSION PUMP, THE CONNECTION DISTAL TO THE PUMP SEGMENT SPONTANEOUSLY DISCONNECTED, REQUIRING IMMEDIATE REPLACEMENT WITH A NEW YELLOW STRIPPED MICROBORE SET. NO OBVIOUS REASON FOR THE DISCONNECTION.
Patient problems: No Information
MAUDE report 7052489 ↗
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- 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 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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