VaPro 72144 (UDI 00610075092642)Recalls & reported problems
Hollister Incorporated · No Touch Urethral Intermittent Catheter, Nelaton · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00610075092642), received between Aug 27, 2024 and Oct 20, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (2 reports).
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 Problem2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Urinary Tract Infection3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT AN END USER WHO HAD BEEN USING THE HOLLISTER VAPRO CATHETERS FOR THE PAST 15 YEARS EXPERIENCED SEVERE URETHRAL IRRITATION AFTER SOME CATHETERS FROM THE PACK COULD NOT BE INSERTED PROPERLY. IT WAS REPORTED THAT THE CATHETER WOULD NOT SLIDE IN THE URETHRA. IT WAS FURTHER REPORTED THAT HE VISITED THE UROLOGIST WHERE HE HAD A BACTERIAL CULTURE DONE AND WAS DIAGNOSED WITH A UTI.
Patient problems: Urinary Tract Infection
MAUDE report 23334974 ↗InjuryOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT SOME OF THE HOLLISTER VAPRO CATHETERS WERE DIFFICULT TO INSERT AND REMOVE AND SOME OF THEM GOT STUCK IN THE URETHRA. IT WAS REPORTED THAT THIS HAS LED TO AN INCREASE IN URINARY TRACT INFECTIONS. IT WAS FURTHER REPORTED THAT THE USER HAS BEEN USING THE PRODUCTS FOR A LONG TIME AND WAS VERY SATISFIED WITH THE NEW COATING, BUT FOR THE PAST FEW MONTHS THESE PROBLEMS HAVE OCCURRED.
Patient problems: Urinary Tract Infection
MAUDE report 23277436 ↗InjuryAug 27, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
FOLLOW-UP 1 TO CORRECT UDI INFORMATION.
Patient problems: Urinary Tract Infection
MAUDE report 20074627 ↗
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.