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HUDSON RCI IPN913853Recalls & reported problems

Teleflex Incorporated · Adult ISO-GARD Breathing Circuit with Dual Heated Limbs and ConchaSmart Column · 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704660619), received between Oct 14, 2021 and Oct 14, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Filling Problem” (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

  • Filling Problem1

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.

  • MalfunctionOct 14, 2021Filling Problem; Filling Problem

    IT WAS REPORTED "CUSTOMER STATES THE CONCHA SMART WATER DID NOT FILL. THE FLOW TUBE WAS UNCLAMPED, AND THE BOTTLE APPEARED TO BE PUNCTURED. NO INJURY OR INTERVENTION. THE "LOW WATER" ALARMED AND COLUMN WAS CHANGED". PATIENT CONDITION REPORTED AS "FINE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12631546 ↗

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Sources and updates

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