Resp-O2 Nasopharyngeal Airways, 28 FR 36279Recalls & reported problems
Dynarex Corporation · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840117323346), received between May 24, 2021 and May 24, 2021 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Aspiration/Inhalation1
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 24, 2021Adverse Event Without Identified Device or Use Problem
EMS REPORT STATES THAT A SUSPECTED OVERDOSE PATIENT ASPIRATED A 28FR NASOPHARYNGEAL AIRWAY THROUGH THE NOSE. IT IS UNCLEAR WHETHER THE ADVERSE EVENT WAS A CONTRIBUTING FACTOR IN THE PATIENT'S LATER DEATH.
Patient problems: Aspiration/Inhalation; Foreign Body In Patient
MAUDE report 11870113 ↗
Other Airway, Nasopharyngeal devices
- Shiley 8888247015Covidien LP · AIRWAY, NASOPHARYNGEAL7 reports
- RUSCH IPN042923Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL5 reports
- RUSCH IPN042918Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042925Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Mallinckrodt 8888247064Covidien LP · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042921Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042213Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL1 report
- Shiley 8888247031Covidien LP · 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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