Parker Flex-Tip H-PSTDL-32Recalls & reported problems
Salter Labs · Parker Endo-Bronch with Standard Tip (Left Double-lumen Endobronchial Tube), PSTDL, 32 Fr, O.D 10.0mm, I.D 3.8mm · Class 2
All models of Parker Flex-Tip (19)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10749065851383), received between Feb 28, 2024 and Feb 28, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (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
- Tear, Rip or Hole in Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 28, 2024Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging
A CUFF TEAR OCCURED DURING INTUBATION OF A PATIENT WITH A SMALL MOUTH. PATIENT WAS EXTUBATED AND RE-INTUBATED WITH A DIFFERENT TUBE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18804830 ↗
Other Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) devices
- HUDSON RCI IPN048996Teleflex Incorporated · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)64 reports
- VivaSight™ 2 DLT Kit 37 Fr - LEFT 412371000Ambu A/S · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 recall10 reports
- HUDSON RCI IPN048995Teleflex Incorporated · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)58 reports
- VivaSight™ 2 DLT Kit 39 Fr - LEFT 412391000Ambu A/S · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 recall6 reports
- VivaSight™ 2 DLT Kit 35 Fr - LEFT 412351000Ambu A/S · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 recall2 reports
- VivaSight™ 2 DLT Kit 41 Fr - LEFT 412411000Ambu A/S · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 recall2 reports
- Portex 198-35LIcu Medical, Inc. · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)48 reports
- Portex 198-37LIcu Medical, Inc. · TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)44 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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