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Bard® Hydro-Glide™ Guidewire 145FS25Recalls & reported problems

C. R. Bard, Inc. · Bard® Hydro-Glide™ Guidewire · Class 1

All models of Bard Hydro-Glide Guidewire (3)

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 00801741053245), received between Sep 6, 2023 and Sep 6, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

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.

  • MalfunctionSep 6, 2023Difficult to Insert; Difficult to Insert

    IT WAS REPORTED THAT A PHYSICIAN IN AN ONLINE SURVEY STATED THAT "NO, THE GUIDEWIRE WAS NOT SUCCESSFUL IN PROVIDING TRANSURETHRAL ACCESS INTO THE URETER¿ BECAUSE "HAD TO DO THE PROCEDURE AGAIN" IN RELATION TO THE HYDROGLIDE GUIDEWIRE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17689452 ↗

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Sources and updates

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