VaPro 72124Recalls & 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 00610075092635), received between Nov 22, 2024 and Nov 22, 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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Hematuria1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 22, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE END USER HAD BEEN CATHETERIZING FOR AT LEAST THE LAST 18 MONTHS AND HAD RECENTLY NOTICED A DIFFERENCE WITH THE LUBRICANT AND SLEEVE OF THE VAPRO CATHETER. IT WAS FURTHER REPORTED THAT THE END USER EXPERIENCED BLEEDING WHEN WITHDRAWING THE CATHETERS FROM HIS URETHRA. IT WAS REPORTED THAT HE WENT TO THE ED AND THEY USED A CLAMP TO CREATE A CLOT. IT WAS ALSO REPORTED THAT HE WAS REFERRED TO A UROLOGIST WHO HAD THE END USER UNDERGO A CT SCAN TO INVESTIGATE HIS REPORT, AND THE CT SCAN SHOWED THE URINE WAS CLEAR AND NO SIGNS OF CANCER. THE UROLOGIST SUGGESTED THE END USER TRY A TIEMAN TIP OR OTHER TYPES OF CATHETERS.
Patient problems: Hematuria
MAUDE report 20758781 ↗
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.