Bard® Interglide™ Intermittent Catheter 431614Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741078033), received between Nov 25, 2020 and Nov 25, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Illegible Information” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 25, 2020Illegible Information; Illegible Information

  IT WAS REPORTED THAT THE PATIENT WAS FRUSTRATED WITH THE LACK OF CLEAR INSTRUCTIONS AND CONCERNED RUNNING WATER OVER THE CATHETER WOULD RENDER IT UNSTERILE AND FINDS IT CONFUSING FOR BARD TO RECOMMEND USE IN THIS MANNER. PATIENT CURRENTLY IN HOSPITAL .PER TROUBLESHOOTING THE MSS STATED THAT RECOMMENDED OPEN PACKAGE AND RUN COLD WATER INTO THE PLASTIC PACKAGE AND WAIT 30 SECONDS TO ACTIVATE SPECIAL NON-SHED SLIPPERY COATING. SUGGESTED TO SPEAK WITH HOSPITAL STAFF ABOUT USE OF ANOTHER CATHETER ESPECIALLY IF BEING TREATED FOR UTI.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10899785 ↗