Trojan™ Premium Latex Condoms Stimulations Ultra Ribbed 00022600940500Recalls & reported problems
Church & Dwight CO., Inc. · For Contraception Plus STI Protection · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600940500), received between Oct 13, 2022 and Oct 13, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Defective Component” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Dec 26, 2025Class IIOpen, Classified
Potential exposure of rodents and rodent activity in the distribution center.
Z-1181-2026 · Root cause: Storage · Recall details · FDA record ↗
Most reported problems
Device problems
- Defective Component1
Patient problems
- Sexually Transmitted Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 13, 2022Defective Component; Defective Component
THIS SPONTANEOUS REPORT (2022-CDW-01502, (B)(6)) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER (AGE AND GENDER UNSPECIFIED) AND WAS RECEIVED VIA FOOD AND DRUG ADMINISTRATION (FDA) MEDWATCH PROGRAM, WHO EXPERIENCED PERMANENT SEXUALLY TRANSMITTED DISEASE (STI) AND A DEFECT IN THE PRODUCT COINCIDENT WITH TROJAN ULTRA RIBBED CONDOMS. THE CONSUMER'S MEDICAL HISTORY AND CONCOMITANT MEDICATIONS WERE NOT REPORTED. ON AN UNSPECIFIED DATE, THE CONSUMER USED TROJAN ULTRA RIBBED CONDOMS FOR THE FIRST SEXUAL EXPERIENCE IN YEARS. ON (B)(6) 2022, THE CONSUMER DEVELOPED A PERMANENT STI AND REALIZED THE DEFECT, WHICH WAS NOT VIEWED AT THE TIME OF THE PRODUCT'S USE. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH THE TROJAN ULTRA RIBBED CONDOMS WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT A PERMANENT STI WAS UNKNOWN. THE OUTCOME OF THE EVENT A DEFECT IN THEM WAS NOT APPLICABLE.
Patient problems: Sexually Transmitted Infection
MAUDE report 15594290 ↗
Other CONDOM devices
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms 00022600642039Church & Dwight CO., Inc. · CONDOM1 recall2 reports
- 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
- DUREX Invisible CondomRB Health (us) LLC · 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 · each recall links to the FDA recall notice
- 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