VaPro 72122Recalls & 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 00610075092598), received between Sep 10, 2024 and Sep 10, 2024 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use 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.
InjurySep 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN END USER FOUND THE EYELETS ON THE CATHETER NOT LARGE ENOUGH TO PASS DEBRIS FROM THE BLADDER WHICH CAUSED THE BLADDER TO NOT EMPTY AND LEAD TO A BLADDER INFECTION. IT WAS REPORTED THAT THE END USER WAS DIAGNOSED WITH A BLADDER INFECTION BY A GENERAL PRACTITIONER AND WAS PRESCRIBED ANTIBIOTICS. IT WAS FURTHER REPORTED THAT THE END USER WAS THEN INSTRUCTED TO CATHETERIZE MORE THAN ONCE A DAY AND TO USE A LARGER FRENCH CATHETER.
Patient problems: Urinary Tract Infection
MAUDE report 20182572 ↗
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.