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RUSCH IPN042921Recalls & reported problems

Teleflex Incorporated · Green Latex Free Naso with Adjustable Flange · Class 1

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 14026704336156), received between Oct 5, 2021 and Oct 5, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Moisture or Humidity Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Moisture or Humidity Problem2

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.

  • MalfunctionOct 5, 2021Moisture or Humidity Problem; Moisture or Humidity Problem

    IT WAS REPORTED "CUSTOMER IS FINDING CONDENSATION INSIDE THE PACKAGING". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12579964 ↗
  • MalfunctionOct 5, 2021Moisture or Humidity Problem; Moisture or Humidity Problem

    IT WAS REPORTED "CUSTOMER IS FINDING CONDENSATION INSIDE THE PACKAGING". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12579951 ↗

Other AIRWAY, NASOPHARYNGEAL devices

All AIRWAY, NASOPHARYNGEAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.