Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms 00022600642145Recalls & reported problems
Church & Dwight CO., Inc. · Class 2
All models of Trojan Premium Latex Condoms Magnum Large Size Condoms (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 00022600642145), received between Nov 11, 2025 and Nov 11, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Device Slipped” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Slipped1
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.
InjuryNov 11, 2025Device Slipped; Device Slipped
THIS SPONTANEOUS CASE WAS REPORTED BY A 32-YEAR-OLD FEMALE CONSUMER FROM THE UNITED STATES OF AMERICA VIA PHONE AND FOLLOWED UP BY TROJAN ECSTASY BREAKAGE SURVEY AND GLOBAL ADE SURVEY. THE REPORTER (CONSUMER) REPORTED USING TROJAN MAGNUM CONDOMS, USED ONE CONDOM IN (B)(6) 2025 FOR INTERCOURSE. AS PER REPORTER, "I WAS USING THE MAGNUM TROJANS AND I HAD INTERCOURSE, AND THE CONDOM SLIPPED OFF INSIDE ME. WE HAD A FEW ISSUES WITH OTHER CONDOMS IN THE BOX NOT ROLLING DOWN PROPERLY. NOW I HAVE IRRITATION IN MY VAGINA, I PEED VERY CLOUDY, I NOTICED STOMACH PAINS WHICH TURNED OUT TO A UTI/ YEAST INFECTION AND STD. THE CONDOM IS STILL INSIDE OF ME. I HAVE TO GO GET A PAP SMEAR TO GET IT REMOVED". THE REPORTER FURTHER REPORTED "THE CONDOMS SLIPPED OFF INSIDE ME DURING INTERCOURSE. AT THE TIME OF GLOBAL ADE SURVEY COMPLETION ((B)(6) 2025), WHEN ASKED "WHAT SYMPTOMS DID YOU EXPERIENCED?", REPORTER STATED "AT LEAST FIVE DAYS AFTER USING THE PRODUCT, IRRITATION IN MY VAGINA, I PEED VERY CLOUDY, I NOTICED STOMACH PAIN WHICH TURNED OUT TO A UTI/ YEAST INFECTION AND STD. WHEN ASKED " HOW LONG DID THE SYMPTOMS LAST? REPORTER STATED, "STILL EXPERIENCING SYMPTOMS THE CONDOM IS STILL INSIDE ME". THE RE
Patient problems: Sexually Transmitted Infection
MAUDE report 23520548 ↗
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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