VaPro Plus 74144-30Recalls & reported problems
Hollister Incorporated · No Touch Urethral Intermittent Catheter with Integrated Collection Bag, Hydrophilic, Straight Tip, Protective Tip and Sleeve · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00610075176144), received between Oct 26, 2021 and Oct 26, 2021 — 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
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.
InjuryOct 26, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN END USER EXPERIENCED A URINARY TRACT BLEED AFTER USING 2 DIFFERENT SKUS OF HOLLISTER'S VAPRO HYDROPHILIC CATHETER. THIS REPORT IS FOR ONE OF THE 2 SKUS. THE BLEEDING LASTED 2 WEEKS. HE SAW SEVERAL MEDICAL PROFESSIONALS TO DIAGNOSE THE SOURCE OF THE BLEEDING BUT THEY WERE UNABLE TO IDENTIFY THE SOURCE. NO TREATMENT WAS REPORTED TO STOP THE BLEEDING. NO BLOOD REPLACEMENT PRODUCTS WERE NEEDED. THE CATHETER WORKED AS INTENDED TO EFFECTIVELY DRAIN THE URINE FROM THE END USER'S BLADDER.
Patient problems: Hematuria
MAUDE report 12699113 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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