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Shiley 8888247056Recalls & reported problems

Covidien LP · Nasopharyngeal Airway · Class 1

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 60884521133124), received between Apr 26, 2018 and Apr 26, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Markings/Labelling Problem1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionApr 26, 2018Device Markings/Labelling Problem; Device Markings/Labelling Problem

    ACCORDING TO THE REPORTER, PRIOR TO USE, THE DEVICE HAD CHINESE LABEL ISSUE. IT WAS STATED THAT 3 BOXES OF THE RECEIVED DEVICE WERE SHOWING DIFFERENT MANUFACTURING DATE. THE CUSTOMER INDICATED NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 7465060 ↗

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.