Blender 10040ARecalls & reported problems
Carefusion Corporation · MICBLNDR,.15-1.0/2-16 LPM,DISS,CE,LO · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10846446002225), received between Jul 9, 2019 and Jan 27, 2022 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Leak/Splash2
- Gas/Air Leak1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 27, 2022Leak/Splash; Leak/Splash
A VYAIRE REPRESENTATIVE REPORTED THE UNIT HAS A LEAK ON THE MICRO-BLENDER COMPONENT. AT THIS TIME, THERE IS NO INFORMATION REGARDING PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13372065 ↗MalfunctionOct 22, 2021Mechanical Problem; Mechanical Problem
THE CUSTOMER REPORTED TO VYAIRE MEDICAL THAT THE MICROBLENDER HAD A MALFUNCTION. AS OF THIS TIME, THERE IS NO INFORMATION ABOUT PATIENT INVOLVEMENT ASSOCIATED WITH THIS REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12685932 ↗MalfunctionSep 22, 2021Leak/Splash; Leak/Splash
A VYAIRE REPRESENTATIVE REPORTED THE UNIT HAS A LEAK ON THE MICOBLENDER COMPONENT. THE VYAIRE REPRESENTATIVE REPORTED THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12515139 ↗InjuryJul 9, 2019Gas/Air Leak; Gas/Air Leak
THE CUSTOMER REPORTED WHILE USING THE BLENDER, THE DEVICE DEVELOPED A VERY LARGE LEAK. THE CUSTOMER REPORTED THE ISSUE OCCURRED AFTER ONE USE AND THEY CANNOT TRACE WHERE THE LEAK IS COMING FROM. THE ISSUE OCCURRED DURING PATIENT-USE. THE CUSTOMER REPORTED THERE IS NO PATIENT CONSEQUENCE ASSOCIATED WITH THE EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8771882 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.