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Vital Signs™ ADU52914Recalls & reported problems

Airlife · Vital Signs™ Adult Anesthesia Breathing Circuit · Class 1

All models of Vital Signs (48)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 10190752121546), received between Feb 3, 2020 and Feb 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Disconnection” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Disconnection1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionFeb 3, 2020Disconnection; Disconnection

    THE CUSTOMER REPORTED THAT THE BREATHING CIRCUIT SEEMS TO COME APART AT THE ELBOW VERY EASILY. AT THIS TIME, PATIENT INVOLVEMENT IS UNKNOWN.

    Patient problems: No Information

    MAUDE report 9661670 ↗

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Sources and updates

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