Vista® US9923FRecalls & reported problems
B. Braun Medical Inc. · VISTA BASIC PUMP IV SET W/ 15 DROP/ML · Class 2
All models of Vista (2)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964838156), received between Sep 10, 2018 and Sep 10, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Infusion or Flow Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Oct 29, 2025Open, Classified
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Z-0715-2026 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Infusion or Flow Problem1
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.
MalfunctionSep 10, 2018Infusion or Flow Problem; Infusion or Flow Problem
AS REPORTED BY THE USER FACILITY: MULTIPLE AIR IN LINE AND DOWNSTREAM OCCLUSION ALARMS OCCURRED. NO VISIBLE BUBBLES OR AIR IN LINE. THESE ALARMS ARE WITH MULTIPLE DRUGS/SOLUTIONS, RATE, VTBI AND MULTIPLE PUMPS. NO INJURY REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7859872 ↗
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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 · each recall links to the FDA recall notice
- 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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