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Vital Signs™ AZFCX7XXXRecalls & reported problems

Airlife · Vital Signs™ Limb-O™ Single Limb 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752123434), received between Mar 29, 2023 and Mar 29, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Leak/Splash” (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

  • Leak/Splash1

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.

  • InjuryMar 29, 2023Leak/Splash; Leak/Splash

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE AZFCX7XXX ANES CIRCUIT, LIMBO, 108 IN, 2L BAG ANESTHESIA BREATHING CIRCUIT DEVELOPED A ¿MAJOR LEAK¿ AFTER BEING IN USE FOR 1 HOUR. THE CIRCUIT WAS REPLACED AND THERE IS NO INFORMATION REGARDING PATIENT HARM OR INJURY ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16640096 ↗

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Sources and updates

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