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HUDSON RCI IPN913814Recalls & reported problems

Teleflex Incorporated · PEDIATRIC BREATHING CIRCUIT WITH COLUMN · Class 2

All models of HUDSON RCI (152)

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 14026704660176), received between Apr 20, 2021 and Apr 20, 2021 — classified as 2 malfunctions.

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

  • Gas/Air Leak2

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.

  • MalfunctionApr 20, 2021Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED "THEY HAD TWO CIRCUITS THAT WOULDN'T PASS THE PRE-USE CHECK ON THE SERVO-I". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11697190 ↗
  • MalfunctionApr 20, 2021Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED "THEY HAD TWO CIRCUITS THAT WOULDN'T PASS THE PRE-USE CHECK ON THE SERVO-I". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11697153 ↗

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Sources and updates

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