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Vital Signs™ B1717XXXRecalls & reported problems

Airlife · Vital Signs™ Pediatric Anethesia 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 10190752124035), received between May 8, 2023 and May 8, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

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 8, 2023Break; Break

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE CIRCUIT, PEDI 108" EXP, 2L LF BAG PASSED PRE-USE CHECK AND WAS USED TO A PATIENT. THE CIRCUIT DID NOT STRETCH AT ALL BUT SIMPLY BROKE. FURTHERMORE, NO HARM WAS DONE TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16886923 ↗

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

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Sources and updates

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