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HUDSON RCI IPN913851Recalls & reported problems

Teleflex Incorporated · SINGLE HEATED DUAL LIMB W DRAIN · 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 14026704660596), received between Jun 29, 2021 and Jun 29, 2021 — classified as 1 malfunction.

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

  • Leak/Splash1

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.

  • MalfunctionJun 29, 2021Leak/Splash; Leak/Splash

    IR WAS REPORTED "EXPIRATORY CUP LEAKING FROM SUCTION PORT". NO PATIENT COMPLICATIONS OR INJURY REPORTED. MULTIPLE ATTEMPTS FOR ADDITIONAL INFORMATION REGARDING ALLEGED ISSUE HAVE BEEN UNSUCCESSFUL. UNKNOWN PATIENT CONDITION AT TIME OF REPORT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12088735 ↗

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Sources and updates

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