RUSCH IPN042925Recalls & reported problems
Teleflex Incorporated · Green Latex Free Naso with Adjustable Flange · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 14026704336194), received between Jan 29, 2025 and Jan 29, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Discolored” (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.
Reports received per month
Most reported problems
Device problems
- Material Discolored1
- Packaging Problem1
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.
MalfunctionJan 29, 2025Packaging Problem; Packaging Problem
IT WAS REPORTED THAT: "THE ITEM ITSELF IS CHANGING COLOR. IT SHOULD BE GREEN BUT SOME ITEMS HAVE TURNED COMPLETELY BLACK, WHILE OTHERS YOU CAN SEE THEM CHANGING FROM GREEN TO BLACK. THE PACKAGING IS FALLING APART. NONE OF THESE PRODUCTS HAVE EXPIRED YET, BUT THE PACKAGING IS RIPPING OPEN AND FALLING APART". ASSOCIATED COMPLAINTS 8040412-2025-00002, 8040412-2025-00003, 8040412-2025-00004 AND 8040412-2025-00005.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21262783 ↗MalfunctionJan 29, 2025Material Discolored; Material Discolored
IT WAS REPORTED THAT: "THE ITEM ITSELF IS CHANGING COLOR. IT SHOULD BE GREEN BUT SOME ITEMS HAVE TURNED COMPLETELY BLACK, WHILE OTHERS YOU CAN SEE THEM CHANGING FROM GREEN TO BLACK. THE PACKAGING IS FALLING APART. NONE OF THESE PRODUCTS HAVE EXPIRED YET, BUT THE PACKAGING IS RIPPING OPEN AND FALLING APART". ASSOCIATED COMPLAINTS 8040412-2025-00002, 8040412-2025-00003, 8040412-2025-00004 AND 8040412-2025-00005.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21262780 ↗
Other AIRWAY, NASOPHARYNGEAL devices
- Shiley 8888247015Covidien LP · AIRWAY, NASOPHARYNGEAL7 reports
- RUSCH IPN042923Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL5 reports
- RUSCH IPN042918Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042921Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Mallinckrodt 8888247064Covidien LP · AIRWAY, NASOPHARYNGEAL2 reports
- Curaplex 2021-15028Bound Tree Medical, LLC · AIRWAY, NASOPHARYNGEAL1 report
- RUSCH IPN042213Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL1 report
- SunMed 1-5075-34Sunmed, 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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