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Bard® Heyman Follower 021118Recalls & reported problems

C. R. Bard, Inc. · Bard® Heyman Follower · 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 00801741075544), 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 17134345 ↗

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.