Blender 10047ARecalls & reported problems
Carefusion Corporation · MICBLNDR,.15-1.0/1.0-10.0 LPM,DISS,CE,LO · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10846446002126), received between May 10, 2019 and May 10, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Material Integrity Problem” (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
- Material Integrity Problem1
Patient problems
- Low Oxygen Saturation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2019Material Integrity Problem; Material Integrity Problem
THE CUSTOMER REPORTED WHILE UNDERGOING EXTRACORPOREAL MEMBRANE OXYGENATION (ECMO) POST OXYGENATOR THERAPY, THE PATIENT'S PARTIAL-ARTERIAL OXYGEN (PA02) LEVEL IS READING SEVENTY (70) MMHG. THE CUSTOMER PERFORMED TROUBLESHOOTING. THE OXYGEN TUBING AND FILTER WAS CHANGED. THE CUSTOMER REPORTED NO IMPROVEMENTS TO THE PATIENT WERE REPORTED WITH THE POST OXYGENATOR PA02 GREATER THAN 500 MMHG. THE CUSTOMER DETERMINED THE MOST LIKELY CAUSE OF THE ISSUE WAS DUE TO THE BLENDER DIAL KNOB. THE CUSTOMER REPORTED IT FOUND TO BE LOOSE. THE CUSTOMER REPORTED VERIFIED THE DEVICE WITH AN ANALYZER CHECK AND REPORTED READING ONLY TWENTY-ONE PERCENT (21%) OXYGEN.
Patient problems: Low Oxygen Saturation
MAUDE report 8599906 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.