Skip to content

GlidePath 5373100Recalls & reported problems

Bard Peripheral Vascular, Inc. · GlidePath 7.5F Long-Term Hemodialysis Catheter, 10 cm · Class 2 · Implant

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 00801741187193), received between Mar 25, 2022 and Mar 25, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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.

Most reported problems

Device problems

  • Deformation Due to Compressive Stress1
  • Restricted Flow rate1

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.

  • MalfunctionMar 25, 2022Restricted Flow rate; Deformation Due to Compressive Stress; Restricted Flow rate; Deformation Due to Compressive Stress

    IT WAS REPORTED THAT POST DIALYSIS CATHETER PLACEMENT PROCEDURE, THE DEVICE ALLEGEDLY HAD A LOW FLOW RATE. IT WAS FURTHER REPORTED THAT THE EXTENSION TUBING OF THE DEVICE WAS NOTED TO BE KINKED. THERE WAS NO REPORTED PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13903578 ↗

Other Catheter, hemodialysis, implanted devices

All Catheter, hemodialysis, implanted devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.