Bard® All Purpose Urethral Catheter 0094100Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741034008), received between Dec 2, 2019 and Dec 21, 2020 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Inadequate Instructions for Healthcare Professional” (3 reports).

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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 21, 2020Inadequate Instructions for Healthcare Professional; Inadequate Instructions for Healthcare Professional

  IT WAS REPORTED THAT THE 9094100 - BRD9094100 - CATH ROBINSON 10FR WAS SHIPPED INSTEAD OF REF (B)(4). IDENTIFIED IN STOCK AND PREVENTED FROM USING.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement

  MAUDE report 11044442 ↗
• MalfunctionDec 21, 2020Inadequate Instructions for Healthcare Professional; Inadequate Instructions for Healthcare Professional

  IT WAS REPORTED THAT THE 9094100 - BRD9094100 - CATH ROBINSON 10FR WAS SHIPPED INSTEAD OF REF 0094100.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement

  MAUDE report 11044441 ↗
• MalfunctionDec 21, 2020Inadequate Instructions for Healthcare Professional; Inadequate Instructions for Healthcare Professional

  IT WAS REPORTED THAT THE 9094100 - BRD9094100 - CATH ROBINSON 10FR WAS SHIPPED INSTEAD OF REF (B)(4). IDENTIFIED IN STOCK AND PREVENTED FROM USING.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement

  MAUDE report 11044434 ↗
• MalfunctionDec 2, 2019Deflation Problem; Deflation Problem; Defective Device

  IT WAS REPORTED THAT WHEN THE RN WAS TREATING A BLADDER PATIENT AND STARTED TO PUSH IN THE SOLUTION, A SMALL SPRAY, ALLEGEDLY, CAME OUT OF THE SIDE OF THE CATHETER A FEW INCHES DOWN FROM THE PROXIMAL END. THE PATIENT NEEDED TO BE RE-CATHETERIZED WITH ANOTHER CATHETER.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 9394853 ↗