VaPro Plus 7700144Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00610075061334), received between Feb 9, 2023 and May 22, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Use of Device 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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 22, 2025Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT A PATIENT WHO SELF-CATHED AT HOME OR BY A NURSE INSERTED THE HOLLISTER VAPRO INTERMITTENT CATHETER WITH THE CAP STILL ON INTO THE BLADDER, LEADING TO THE CREATION OF A 4 CM BLADDER STONE. IN ADDITION, IT WAS REPORTED THAT IT ALSO CAUSED LOWER URINARY TRACT SYMPTOMS WORSE THAN USUAL, RESULTING IN REPEATED URINARY TRACT INFECTIONS. IT WAS FURTHER REPORTED THAT THIS ULTIMATELY REQUIRED SURGERY UNDER GENERAL ANESTHESIA TO REMOVE THE BLADDER STONE, A CT SCAN, AND A 3-DAY HOSPITALIZATION.

  Patient problems: Urinary Tract Infection; Urolithiasis

  MAUDE report 22069610 ↗
• InjuryFeb 9, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AN END USER REPORTED THAT THE VAPRO PLUS INTERMITTENT HYDROPHILIC URINARY CATHETER WAS DIFFICULT FOR HIM TO INSERT AND REMOVE. HE REPORTED THAT WHEN HE REMOVED IT, A BLOOD VESSEL WAS INJURED AND HE BLED. HE REPORTED HE WAITED A FEW DAYS AND SAW A DOCTOR BECAUSE THE BLEEDING WOULDN'T STOP. HE SAID HE SAW A UROLOGIST WHO ARRANGED FROM HIM TO BE ADMITTED TO THE HOSPITAL. THE END USER DID NOT REPORT IF ANY MEDICAL TREATMENT WAS NEEDED FOR THE BLEEDING TO STOP. THE END USER SAID HE WAITED UNTIL THE NEXT DAY TO GO TO THE HOSPITAL. THE END USER FURTHER REPORTED THAT THE NIGHT BEFORE HE WENT TO THE HOSPITAL, HE DEVELOPED A FEVER AND SEPSIS. THE END USER DID NOT REPORT WHAT WAS THE SOURCE OF THE SEPSIS. WHILE IN THE HOSPITAL, THE END USER REPORTED THAT HE HAD AN INDWELLING CATHETER AND WAS ON ANTIBIOTICS. THE END USER REPORTED THAT THIS WAS ABOUT A MONTH AGO. HE REPORTS THAT HE IS FEELING FINE NOW.

  Patient problems: Genital Bleeding; Sepsis

  MAUDE report 16333779 ↗