Shiley 8888247031Recalls & reported problems
Covidien LP · Nasopharyngeal Airway · Class 1
All models of Shiley (387)
Data updated Oct 16, 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 60884521133100), received between Jan 14, 2026 and Jan 14, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Integrity 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.
MalfunctionJan 14, 2026Material Integrity Problem
IT WAS REPORTED THAT AFTER EXTUBATION, THE PATIENT EXPERIENCED TONGUE FALL-BACK AND A SLIGHT DECREASE IN OXYGEN SATURATION TO 92% AP PROXIMATELY 2-3 MINUTES. A NASOPHARYNGEAL AIRWAY WAS PLACED, BUT THE PACKAGING WAS FOUND TO BE DAMAGED, IT WAS REPLACED WITHOUT ISSUE BUT PROLONGED THE PATIENT'S PERIOD OF HYPOXIA. THE PATIENT'S OXYGEN SATURATION IMPROVED AND RETURNED TO THE WARD SMOOTHLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24072881 ↗
Other AIRWAY, NASOPHARYNGEAL devices
- Shiley 8888247015Covidien LP · AIRWAY, NASOPHARYNGEAL7 reports
- RUSCH IPN042923Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL5 reports
- RUSCH IPN042925Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042918Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042921Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Mallinckrodt 8888247064Covidien LP · AIRWAY, NASOPHARYNGEAL2 reports
- Resp-O2 Nasopharyngeal Airways, 28 FR 36279Dynarex Corporation · Airway, Nasopharyngeal1 report
- Curaplex 2021-15028Bound Tree Medical, LLC · AIRWAY, NASOPHARYNGEAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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