VaPro Plus Pocket 71124-30Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00610075054008), received between Mar 25, 2022 and Aug 4, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem 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. 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.

• InjuryAug 4, 2025Material Too Rigid or Stiff; Patient Device Interaction Problem; Material Too Rigid or Stiff; Patient Device Interaction Problem

  IT WAS REPORTED THAT AN END USER EXPERIENCED INTERNAL TRAUMA WHILE USING THE HOLLISTER VAPRO PLUS POCKET INTERMITTENT URINARY CATHETER TO CATHETERIZE HER MITROFANOFF CONTINENT URINARY CHANNEL. IT WAS FURTHER REPORTED THAT THE CATHETER WAS SIGNIFICANTLY STIFFERAND LESS FLEXIBLE, RESULTING IN PAINFUL INSERTIONS AND INJURIES THAT REQUIRED EMERGENCY CARE. IT WAS REPORTED THAT THE END USER EXPERIENCED MULTIPLE FALSE PASSAGES, BLEEDING, INTERNAL TRAUMA, AND REPEATED VISITS AND PROCEDURES AT THE (B)(6). IT WAS REPORTED THAT THE END USER NEEDED TO WEAR A FOLEY BAG FOR TWO MONTHS TO ALLOW TIME TO HEAL. IT WAS ADDITIONALLY REPORTED THAT IN THE FIRST OR SECOND WEEK OF JUNE SHE HAD COMPLETE BLOCKAGE AND HAD TO HAVE A FOLEY INSERTED TO ALLOW THE FALSE PASSAGES TO HEAL. IT WAS FURTHER REPORTED THAT THE END USER IS A LONG-TERM USER OF THE ORIGINAL VAPRO PLUS POCKET CATHETERS AND HAD NO ISSUES UNTIL THE NEWER MODEL WAS INTRODUCED.

  Patient problems: Pain

  MAUDE report 22700373 ↗
• InjuryMar 25, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  A HOSPITAL REPORTED THAT A HOLLISTER VAPRO PLUS POCKET INTERMITTENT URINARY CATHETER CAUGHT ON REMOVAL AFTER BLADDER DRAINAGE AND REQUIRED MORE FORCE THAN NORMAL TO REMOVE; THE COATING WAS STICKY AND DRY, WHICH REPORTEDLY CAUSED THE PATIENT TO EXPERIENCE HEMATURIA. THEY ALSO REPORTED THAT THE PATIENT WAS UNWELL FOR 5 DAYS AFTER THE REPORT AND IV ANTIBIOTICS WERE PRESCRIBED FOR THE HEMATURIA. THE HOSPITAL FURTHER REPORTED THAT THERE WERE NO LONG TERM PATIENT ISSUES OR PRESCRIPTIONS FROM THE INCIDENT.

  Patient problems: Hematuria

  MAUDE report 13900418 ↗