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Vital Signs™ 5037AERecalls & 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
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752118461), received between May 16, 2023 and May 17, 2023 — classified as 2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Leak/Splash2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 17, 2023Leak/Splash; Leak/Splash

    IT WAS REPORTED TO VYAIRE MEDICAL THAT ANES CIRCUIT, ADULT, 60 IN CORR, 3L BAG HAD A LEAK AFTER PATIENT USE. FURTHERMORE, THERE IS NO INFORMATION REGARDING PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16949956 ↗
  • MalfunctionMay 16, 2023Leak/Splash; Leak/Splash

    IT WAS REPORTED TO VYAIRE MEDICAL THAT ANES CIRCUIT, ADULT, 60 IN CORR, 3L BAG HAD A LEAK DURING PATIENT USE. FURTHERMORE, THE CUSTOMER CONFIRMED NO HARM WAS DONE TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16937932 ↗

Other Circuit, breathing (w connector, adaptor, y piece) devices

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Sources and updates

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