Blender 03803TRecalls & reported problems
Carefusion Corporation · MICBLNDR,W/O HOSE,3 OUTLET,H/L · Class 2
All models of Blender (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10846446002256), received between Nov 19, 2019 and Sep 2, 2020 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (2 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
- Mechanical Problem2
Patient problems
- No Information1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 2, 2020Mechanical Problem; Mechanical Problem
THE CUSTOMER REPORTED THAT THE FIO2 (FRACTION OF INSPIRED OXYGEN) OF THE BLENDER IS OUT OF SPECIFICATION. AT THIS TIME, THERE IS NO INFORMATION ABOUT PATIENT INVOLVEMENT.
Patient problems: No Information
MAUDE report 10485774 ↗InjuryNov 19, 2019Mechanical Problem; Mechanical Problem
IT WAS REPORTED TO VYAIRE THAT THE MICROBLENDER IS ALARMING WHILE THE 2 GASES WERE CONNECTED. THE CUSTOMER ADVISED THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THIS EVENT.
Patient problems: No Patient Involvement
MAUDE report 9344327 ↗
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- Sechrist Industries, Inc. 3500CP-G4Sechrist Industries, Inc. · Mixer, Breathing Gases, Anesthesia Inhalation3 reports
- Precision Medical Blender PM5300Precision Medical, Inc. · Mixer, Breathing Gases, Anesthesia Inhalation3 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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