RUSCH IPN041444Recalls & reported problems
Teleflex Incorporated · PREFORMED AGT NASAL ENDOTRACHEAL TUBE - MURPHY EYE, HIGH VOLUME, LOW PRESSURE CUFF - STERILE PACK · Class 2
All models of RUSCH (220)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026704341181), received between Feb 4, 2026 and Feb 4, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Puncture/Hole” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1952-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Puncture/Hole1
- 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.
MalfunctionFeb 4, 2026Material Puncture/Hole
IT WAS REPORTED THAT: "DURING A DENTAL CASE THE ET TUBE WAS REMOVED THEY NOTICED A HOLE IN THE TUBE. ONLY 1 WAS USED ON A PATIENT, THE OTHERS WERE NOT USED ON PATIENTS. ONCE THEY REALIZED THERE WAS A HOLE, THEY CHECKED THE REMAINING PRODUCTS IN THE BOX AND DISCOVERED THAT THEY ALL HAD HOLES. ISSUE WAS RESOLVED BY USING A TUBE FROM ANOTHER BOX/LOT THE NEXT TIME. NO PATIENT HARM OR CONSEQUENCE." ASSOCIATED COMPLAINTS 8040412-2026-00013.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257233 ↗MalfunctionFeb 4, 2026Tear, Rip or Hole in Device Packaging
IT WAS REPORTED THAT: "DURING A DENTAL CASE THE ET TUBE WAS REMOVED THEY NOTICED A HOLE IN THE TUBE. ONLY 1 WAS USED ON A PATIENT, THE OTHERS WERE NOT USED ON PATIENTS. ONCE THEY REALIZED THERE WAS A HOLE, THEY CHECKED THE REMAINING PRODUCTS IN THE BOX AND DISCOVERED THAT THEY ALL HAD HOLES. ISSUE WAS IDENTIFIED IN INVENTORY. NO PATIENT INVOLVED" ASSOCIATED COMPLAINTS 8040412-2026-00010.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257201 ↗
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 · each recall links to the FDA recall notice
- 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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