Outlook® V7490Recalls & reported problems
B. Braun Medical Inc. · Outlook® Pump Blood Administration Set · Class 2
All models of Outlook (25)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04046964189401), received between Nov 22, 2016 and Feb 18, 2021 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (5 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
- Device Operates Differently Than Expected5
- Contamination /Decontamination Problem1
Patient problems
- No Consequences Or Impact To Patient5
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2021Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT THE SET WAS SPIKED AND NORMAL SALINE WAS PRIMED THROUGH THE TUBING AND THE NURSE NOTICED A WHITE PIECE OF PLASTIC IN THE CASSETTE. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11344217 ↗MalfunctionNov 22, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
AS REPORTED BY USER FACILITY: EVENT 5. IV TUBE IS LEAKING BLOOD DURING TRANSFUSION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6120471 ↗MalfunctionNov 22, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
AS REPORTED BY USER FACILITY: EVENT 4. IV TUBE IS LEAKING BLOOD DURING TRANSFUSION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6120467 ↗MalfunctionNov 22, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
AS REPORTED BY USER FACILITY: EVENT 3. IV TUBE IS LEAKING BLOOD DURING TRANSFUSION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6120448 ↗MalfunctionNov 22, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
AS REPORTED BY USER FACILITY: EVENT 2. IV TUBE IS LEAKING BLOOD DURING TRANSFUSION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6120444 ↗MalfunctionNov 22, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
AS REPORTED BY USER FACILITY: EVENT 1. IV TUBE IS LEAKING BLOOD DURING TRANSFUSION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6120437 ↗
Other Set, administration, intravascular devices
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- 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 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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