RUSCH IPN042918Recalls & 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 14026704336125), received between Dec 24, 2025 and Dec 24, 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
- Tear, Rip or Hole in Device Packaging1
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.
MalfunctionDec 24, 2025Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging
IT WAS REPORTED THAT: "GREEN NASAL TRUMPETS BEGAN TURNING BLACK AND PACKAGING WAS COMPROMISED, TEARING APART WITH THE SLIGHTEST TOUCH. PARTS OF PRODUCT THAT CHANGED COLOR ALSO HARDENED WHICH REDUCED THE FLEXIBILITY OF THE TUBE." ASSOCIATED COMPLAINTS (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23887393 ↗MalfunctionDec 24, 2025Material Discolored; Material Discolored
IT WAS REPORTED THAT: "GREEN NASAL TRUMPETS BEGAN TURNING BLACK AND PACKAGING WAS COMPROMISED, TEARING APART WITH THE SLIGHTEST TOUCH. PARTS OF PRODUCT THAT CHANGED COLOR ALSO HARDENED WHICH REDUCED THE FLEXIBILITY OF THE TUBE." ASSOCIATED COMPLAINTS 8040412-2025-00143, 8040412-2025-00144, 8040412-2025-00276, 8040412-2025-00275 AND 8040412-2025-00145.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23887385 ↗
Other AIRWAY, NASOPHARYNGEAL devices
- Shiley 8888247015Covidien LP · AIRWAY, NASOPHARYNGEAL7 reports
- RUSCH IPN042923Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL5 reports
- RUSCH IPN042921Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Mallinckrodt 8888247064Covidien LP · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042925Teleflex Incorporated · 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.