Trojan™ Lubricants Premium Collection Arouses & Releases™* 00022600959632Recalls & reported problems
Church & Dwight CO., Inc. · Class 2
Data updated Oct 18, 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 00022600959632), received between Jul 11, 2023 and Jul 11, 2023 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Abnormal Vaginal Discharge1
- Erythema1
- Inflammation1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 11, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS SPONTANEOUS REPORT (2023-CDW-01038, 007801819A) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A 25-YEAR-OLD FEMALE CONSUMER WHO EXPERIENCED AN INFLAMED VAGINA/LABIA MINORA, SORENESS, PAIN, REDNESS, AND DISCHARGE AND WAS UNABLE TO WORK AFTER USING THE TROJAN AROUSES AND RELEASES PERSONAL LUBRICANT. THE CONSUMER'S MEDICAL HISTORY WAS NOT REPORTED. THE CONCOMITANT MEDICATIONS INCLUDED TYLENOL (ACETAMINOPHEN), IBUPROFEN, BENADRYL (DIPHENHYDRAMINE), LIDOCAINE, AND AMOXICILLIN. ON (B)(6) 2023 (SATURDAY), THE CONSUMER USED TROJAN AROUSES AND RELEASES PERSONAL LUBRICANT (NOT A LOT WAS USED) TOPICALLY (FOR 1 DAY). ON (B)(6) 2023, SHE EXPERIENCED AN INFLAMED VAGINA, SORENESS, REDNESS, DISCHARGE, AND PAIN IN HER LABIA MINORA. SHE WALKED IN AT URGENT CARE FOR HER TREATMENT AND GOT ADMITTED TO THE HOSPITAL ON (B)(6) 2023 (FRIDAY). DUE TO THESE SYMPTOMS, SHE WAS UNABLE TO WORK. AT THE TIME OF THIS REPORT, SHE WAS STILL EXPERIENCING VAGINAL REDNESS, INFLAMMATION, SORENESS, AND PAIN. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH TROJAN AROUSES AND RELEASES PERSONAL LUBRICANT WAS NOT APPLICABLE. THE OUTCOME OF THE EVENTS WAS NOT RECOVERED.
Patient problems: Abnormal Vaginal Discharge; Erythema; Inflammation; Pain
MAUDE report 17296200 ↗
Other Lubricant, personal devices
- Astroglide Ultra Gentle Gel 015594011035Biofilm, Inc · Lubricant, Personal1 report
- KY Touch 2-in-1 Massage Creme & Pleasure Gel Personal LubricantRB Health (us) LLC · Lubricant, personal1 report
- Replens™ Long-Lasting Vaginal Moisturizer 00022600001041Church & Dwight CO., Inc. · Lubricant, personal1 report
- KY Warming Jelly 00067981089479Reckitt Benckiser LLC · Lubricant, Personal1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page