VaPro Pocket 70124 (UDI 00610075093069)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00610075093069), received between May 9, 2025 and Aug 21, 2025 — classified as 3 injuries.

The most frequently reported specific device problem is “Difficult to Insert” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryAug 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE END USER EXPERIENCED AN INCREASE IN URINARY TRACT INFECTIONS (UTIS) OVER THE PAST FEW MONTHS FOLLOWING THE PRODUCT UPDATE FROM THE HOLLISTER VAPRO POCKET TO THE HYDRABALANCE VERSION. SPECIFICALLY, IT WAS REPORTED THAT THE END USER EXPERIENCED A TOTAL OF THREE UTIS WITHIN THE PAST TWO MONTHS. IT WAS FURTHER REPORTED THAT THE END USER FIRST NOTICED A CHANGE IN THE CATHETER PRODUCT APPROXIMATELY THREE MONTHS AGO, AND THE ONSET OF UTIS BEGAN SHORTLY THEREAFTER, APPROXIMATELY 8 TO 10 WEEKS AGO. IT WAS ALSO REPORTED THAT THE END USER HAS BEEN PERFORMING INTERMITTENT CATHETERIZATION FOR APPROXIMATELY 3.5 TO 4 YEARS AND USES THIS SKU OF CATHETERS IN THE MORNING AND AT BEDTIME. WHILE IT WAS REPORTED THAT THE END USER HAS EXPERIENCED UTIS IN THE PAST, THE END USER REPORTED THAT THE FREQUENCY APPEARS TO HAVE INCREASED IN RECENT MONTHS. IT WAS ADDITIONALLY REPORTED THAT THE END USER HAS BEEN INTERMITTENTLY TREATED WITH ANTIBIOTICS, BUT THE END USER DOES NOT FEEL THAT THE TREATMENT HAS BEEN EFFECTIVE.

  Patient problems: Urinary Tract Infection

  MAUDE report 22859924 ↗
• InjuryAug 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT NOTICED THAT THE HOLLISTER VAPRO POCKET INTERMITTENT CATHETER TUBING IS NOW CLEAR AND HAS BEEN SUFFERING FROM A URINARY TRACT INFECTION. IT WAS FURTHER REPORTED THAT THIS MAY NOT BE RELATED BUT HE NEEDS TO SEEK AN ALTERNATIVE URETHRAL CATHETER.

  Patient problems: Urinary Tract Infection

  MAUDE report 22842356 ↗
• InjuryMay 9, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT AN END USER WHO HAD BEEN USING THE VAPRO POCKET INTERMITTENT URETHRAL CATHETER FOR 1 YEAR RECEIVED THE VAPRO HYDRABALANCE PRODUCT AND HAD BEEN USING IT FOR 2 DAYS WHEN HE FOUND IT DIFFICULT TO INSERT AND EXPERIENCED STINGING ON WITHDRAWAL. IT WAS FURTHER REPORTED THAT HE ADJUSTED HIS CATHETERIZATION TECHNIQUE, AND THE ISSUE RESOLVED. IT WAS THEN REPORTED THAT HE DEVELOPED A UTI AND WITH THAT THERE WAS SOME DISCOMFORT. ADDITIONALLY, IT WAS REPORTED THAT HE STARTED ANTIBIOTICS.

  Patient problems: Urinary Tract Infection

  MAUDE report 21992835 ↗