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Parker Flex-Tip H-PTCL-30Recalls & reported problems

Salter Labs · Endotracheal Tube, DEHP-free, Low Pressure, Polyurethane Cuff, no Murphy eyes, (PTCL), Parker, 3.0mm · Class 2

All models of Parker Flex-Tip (19)

Data updated Oct 18, 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 10749065161307), received between Jan 19, 2018 and Jan 19, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Issue” (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 18, 2026.

Most reported problems

Device problems

  • Device Issue1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 19, 2018Device Issue; Device Issue

    CUSTOMER REPORTS THAT THE PILOT CUFF AND TUBE BECAME DISCONNECTED FROM THE BODY OF THE ENDOTRACHEAL TUBE. ET TUBE WAS CHANGED OUT SUCCESSFULLY. NO PATIENT INJURY WAS REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7207081 ↗

Other Tube, Tracheal (W/Wo Connector) devices

All Tube, Tracheal (W/Wo Connector) devices →

Sources and updates

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