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Blender 10042A (UDI 10190752174726)Recalls & reported problems

Vyaire Medical, Inc. · MICROBLENDER, 1.0-10.0/2-16 LPM, DISS, CE, LO · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752174726), received between May 24, 2022 and May 24, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical 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

  • Mechanical Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 24, 2022Mechanical Problem; Mechanical Problem

    THE CUSTOMER REPORTED TO VYAIRE MEDICAL THAT THE MICROBLENDER COMPONENT WAS NEEDING A TUBING THAT GOES FROM THE FLOW METER TO THE BLENDER AS THE FLOW METER TUBING WAS LEAKING. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14492473 ↗

Other Mixer, breathing gases, anesthesia inhalation devices

All Mixer, breathing gases, anesthesia inhalation devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.