VaPro 72102Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00610075081202), received between Nov 23, 2021 and Nov 23, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryNov 23, 2021Material Fragmentation; Material Fragmentation

  IT WAS REPORTED THAT AN END USER HAD BEEN COMPLAINING ABOUT ABDOMINAL PAIN FOR THE PAST 6 MONTHS. SHE SAW HER GP WHO REFERRED HER BACK TO UROLOGY CONSULTANT. THE CONSULTANT PERFORMED A SCAN WHERE THEY SAW SOMETHING INSIDE THE BLADDER WHICH THEY THOUGH COULD BE MUCUS DEBRIS OR BLOOD. THEY ALSO PROVIDED INTRAVENOUS ANTIBIOTIC TREATMENT. A LITTLE BIT LATER, THEY INSERTED A CAMERA AND REMOVED FROM HER BLADDER A 3.8 CM LONG FRAGMENT WHICH THEY REPORTED TO BE THE VAPRO HYDROPHILIC CATHETER'S NO TOUCH SLEEVE. SHE HAD BEEN EXPERIENCING BLEEDING AND CLOTS IN HER URINE WHICH IMMEDIATELY STOPPED FOLLOWING THE REMOVAL OF THE FRAGMENT. THE FRAGMENT THAT WAS REMOVED WAS NOT SAVED; THEREFORE HOLLISTER CANNOT INDEPENDENTLY CONFIRM THE FRAGMENT IDENTIFICATION.

  Patient problems: Abdominal Pain

  MAUDE report 12860296 ↗