VaPro Pocket 70144-30Recalls & reported problems
Hollister Incorporated · No Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve · Class 2
Data updated Oct 16, 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 00610075067978), received between Nov 18, 2025 and Nov 18, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Physical Resistance/Sticking1
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.
InjuryNov 18, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
IT WAS REPORTED THAT AN END USER RECEIVED EXPIRED BOXES OF VAPRO POCKET INTERMITTENT CATHETERS. PRIOR TO NOTICING THE EXPIRATION DATE, THE USER UTILIZED THE PRODUCTS FOR SELF-CATHETERIZATION. IT WAS FURTHER REPORTED THAT DURING USE, SOME CATHETERS WERE OBSERVED TO HAVE INADEQUATE LUBRICATION UPON OPENING, WITH THE ISSUE BECOMING EVIDENT UPON REMOVAL WHEN THE CATHETERS SNAGGED ON THE URETHRA. SUBSEQUENTLY, IT WAS REPORTED THAT THE USER DEVELOPED A URINARY TRACT INFECTION.
Patient problems: Urinary Tract Infection
MAUDE report 23582072 ↗
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 82164Hollister Incorporated · CATHETER, URETHRAL1 recall1 report
- Onli 82144Hollister 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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