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HUDSON RCI IPN913837Recalls & reported problems

Teleflex Incorporated · Adult ConchaSmart Breathing Circuit with Dual Heated · Class 2

All models of HUDSON RCI (152)

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 14026704660770), received between Sep 14, 2021 and Sep 14, 2021 — classified as 1 injury.

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

  • Gas/Air Leak1

Patient problems

  • Low Oxygen Saturation1

Recent adverse event reports

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

  • InjurySep 14, 2021Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED "RT [RESPIRATORY THERAPIST] FOUND CIRCUIT WITH LEAK. APPARENTLY, THE HEATED WIRE MELTED THE CIRCUIT HOSE AND CREATED THE LEAK. IT IS UNKNOWN IF THE PATIENT WAS LAYING ON THE TUBING OR IF THE TUBING WAS COVERED BY BEDDING OR OTHER". IT WAS REPORTED THE CIRCUIT WAS CHANGED. PATIENT CONDITION REPORTED AS "FINE".

    Patient problems: Low Oxygen Saturation

    MAUDE report 12470860 ↗

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Sources and updates

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