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Woven Filiform Straight Tip 021906Recalls & reported problems

C. R. Bard, Inc. · Woven Filiform Straight Tip · Class 1

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 00801741073106), received between Jun 15, 2023 and Jun 15, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling Problem” (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

  • Device Handling Problem1
  • Fitting Problem1

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.

  • MalfunctionJun 15, 2023Fitting Problem; Device Handling Problem; Fitting Problem; Device Handling Problem

    IT WAS REPORTED THAT CUSTOMER HAD BARD FOLLOWERS AND FILIFORMS BUT THE TIPS WERE NOT CONNECTING. (PCN 021114 , PCN 021112 , PCN 021116 , PCN 021118 , PCN 021120 , PCN 021122 , PCN 021124 , PCN 021316 , PCN 021100, PCN 021905 , PCN 021906 , PCN 022105).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17134346 ↗

Other FILIFORM AND FILIFORM FOLLOWER devices

All FILIFORM AND FILIFORM FOLLOWER devices →

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