RUSCH IPN041457Recalls & reported problems
Teleflex Incorporated · NASAL SAFETY SILK TRACHEAL TUBE - MURPHY EYE -WITH CUFF-STERILE PACK. · Class 2
All models of RUSCH (220)
Data updated Oct 16, 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 04026704325634), received between Feb 6, 2025 and Mar 18, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Gas/Air Leak” (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
- Gas/Air Leak1
- Inflation Problem1
- Physical Resistance/Sticking1
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.
MalfunctionMar 18, 2025Inflation Problem; Physical Resistance/Sticking; Inflation Problem; Physical Resistance/Sticking
IT WAS REPORTED THAT: "INCIDENT OCCURRED ON (B)(6) 2025. PATIENT WAS INTUBATED; PILOT BALLOON WAS UNABLE TO INFLATE (WALLS OF THE PILOT BALLOON STUCK TOGETHER). AS A RESULT, TUBE WAS REMOVED AND INTUBATION REPEATED. THERE WERE NO CLINICAL CONSEQUENCES OR DESATURATION FOR THE PATIENT. THERE WAS ONLY A DELAY IN TREATMENT. THE PATIENT LEFT THE HOSPITAL ON THE DAY AS SCHEDULED ON (B)(6) 2025."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21629149 ↗MalfunctionFeb 6, 2025Gas/Air Leak; Gas/Air Leak
IT WAS REPORTED THAT "THE AIR LEAKING WAS FOUND IN THE LATE PHASE OF SURGERY, AND DOCTOR RETRACTED IT. PATIENT WAS FINE". AT THE TIME OF THIS REPORT, THE CUSTOMER HAS NOT RETURNED OUR REQUESTS FOR ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21323451 ↗
Other Tube, tracheal (w/wo connector) devices
- Shiley 18875Covidien LP · Tube, tracheal (w/wo connector)4 deaths570 reports
- RUSCH IPN041476Teleflex Incorporated · Tube, tracheal (w/wo connector)10 recalls0 reports
- Shiley 18775Covidien LP · Tube, tracheal (w/wo connector)489 reports
- Shiley 18770Covidien LP · Tube, tracheal (w/wo connector)2 deaths434 reports
- Shiley 18880Covidien LP · Tube, tracheal (w/wo connector)2 deaths370 reports
- Shiley 18780Covidien LP · Tube, tracheal (w/wo connector)3 deaths286 reports
- Shiley 18770SCovidien LP · Tube, tracheal (w/wo connector)273 reports
- Shiley 18780SCovidien LP · Tube, tracheal (w/wo connector)251 reports
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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