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Vital Signs™ AFN52024Recalls & 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752121782), received between Aug 8, 2022 and Aug 8, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Loose or Intermittent Connection1

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.

  • MalfunctionAug 8, 2022Loose or Intermittent Connection; Loose or Intermittent Connection

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE CONNECTION BETWEEN THE FILTER AND ETT/MASK WAS LOOSE CAUSING THE PATIENT TO BE DISCONNECTED FROM THE AFN52024 - ANES CIRCUIT, ADULT, 72 IN LIMBO, 3L BAG. THE STAFF SUPPORTED THE CONNECTION WITH THEIR HAND JUST TO ENSURE THE PATIENT STAYS ON THE BREATHING MACHINE. THERE WERE NO REPORTS OF INJURY/HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15186851 ↗

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Sources and updates

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