Trojan™ Premium Latex Condoms Ultra Ribbed Value Pack 00022600949510Recalls & 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 00022600949510), received between Jul 11, 2025 and Jul 11, 2025 — 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
- Dysuria1
- Hematuria1
- Pain1
- Unspecified Tissue Injury1
- 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.
InjuryJul 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS SPONTANEOUS REPORT (2025-CDW-01121, (B)(6)) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A 24-YEAR-OLD FEMALE CONSUMER VIA CHAT AND FOLLOWED UP BY A SURVEY, WHO REPORTED IT CAUSED BODILY INJURY AND URINARY TRACT INFECTION AFTER USING THE TROJAN LATEX ULTRA RIBBED LUBRICATED CONDOMS. ON 24-APR-2025, THE CONSUMER REPORTED INITIATING THE USE OF TROJAN LATEX ULTRA RIBBED LUBRICATED CONDOMS ONCE FOR BIRTH CONTROL AS PER THE DIRECTION OF HER PRIMARY CARE RECOMMENDATION. LATER, THE CONSUMER REPORTED VIA CHAT THAT SHE EXPERIENCED BODILY INJURY THAT OCCURRED ON (B)(6) 2025. SHE ALLEGED THAT THE PRODUCT CAUSED URINARY TRACT INFECTION. ADDITIONALLY, THE CONSUMER REPORTED IN THE SURVEY ON JUNE 30, 2025, "VERY QUICK AFTER USING, BURNING, PAIN WHILE AFTER URINATING. BLOOD IN URINE. SIDE PAIN." THE CONSUMER STATED SHE DID SEEK MEDICAL ATTENTION FROM TWO DIFFERENT HOSPITALS AND WAS ADMITTED INTO THE HOSPITAL. SHE HAD ULTRASOUND, BLOOD CP AND URINE REVALUATION DONE AND RECEIVED MEDICATION (IV/ORAL) (UNSPECIFIED). HER SYMPTOMS LASTED 2 WEEKS. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH TROJAN LATEX ULTRA RIBBED LUBRICATED CONDOMS WAS NOT APPLICABLE. THE OUTCOME OF THE EV
Patient problems: Burn(s); Dysuria; Hematuria; Pain; Unspecified Tissue Injury; Urinary Tract Infection
MAUDE report 22480095 ↗
Other CONDOM devices
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms 00022600642039Church & Dwight CO., Inc. · CONDOM1 recall2 reports
- Trojan™ Premium Latex Condoms Stimulations Ultra Ribbed 00022600940500Church & Dwight CO., Inc. · CONDOM1 recall1 report
- Trojan™ Premium Latex Condoms Sensitivity Ultra Thin 00022600926207Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms Her Pleasure™ Sensations 00022600973201Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms ENZ™ Armor Spermicidal Lubricant 00022600931508Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ ENZ™ Latex Lubricated Condoms 00022600930501Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms BareSkin™ Value Pack 00022600998532Church & Dwight CO., Inc. · CONDOM3 reports
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin 00022600646143Church & Dwight CO., Inc. · CONDOM2 reports
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.
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