VaPro 72164Recalls & reported problems
Hollister Incorporated · No Touch Urethral Intermittent Catheter, Nelaton · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00610075092659), received between Feb 20, 2026 and Feb 20, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction 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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Urinary Tract Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 20, 2026Patient Device Interaction Problem
IT WAS REPORTED THAT AN END USER WHO WAS USING THE HOLLISTER VAPRO CATHETERS HAD TROUBLE INSERTING TWO OF THE CATHETERS BUT WAS SUCCESSFUL CATHETERIZING WITH THE THIRD ONE. IT WAS REPORTED THAT SEVERAL DAYS LATER, HE WAS RUSHED TO HOSPITAL AND WAS TOLD BY THE DOCTOR HE HAD UROSEPSIS DUE TO CATHETER USE. IN ADDITION, IT WAS REPORTED THAT THERE WERE NO ISSUES WITH THE LUBRICATION, BUT IT WAS JUST TECHNIQUE BEING THAT THIS WAS THE FIRST TIME THIS END USER HAD PERFORMED SELF-CATHETERISATION.
Patient problems: Urinary Tract Infection
MAUDE report 24400689 ↗
Other CATHETER, URETHRAL devices
- Bardex® All-Silicone Foley Catheter 165814C. R. Bard, Inc. · CATHETER, URETHRAL275 reports
- GENTLECATH 421911Convatec, Purchasing Department · Catheter, Urethral234 reports
- GENTLECATH 421910Convatec, Purchasing Department · Catheter, Urethral122 reports
- CURE CATHETER M16CConvatec, Purchasing Department · Catheter, Urethral95 reports
- GENTLECATH 421909Convatec, Purchasing Department · Catheter, Urethral66 reports
- BD Intermittent RTU14FHangzhou Bever Medical Devices Co., Ltd. · Catheter, Urethral1 recall3 reports
- Onli 82124Hollister Incorporated · CATHETER, URETHRAL1 recall1 report
- Onli 82164Hollister Incorporated · CATHETER, URETHRAL1 recall1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.