Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms 00022600642039Recalls & reported problems
Church & Dwight CO., Inc. · For Contraception Plus STI Protection · 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
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00022600642039), received between Aug 21, 2025 and Nov 30, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 reports).
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.
Reports received per month
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
- Break2
Patient problems
- Sexually Transmitted Infection2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 30, 2025Break; Break
THIS SPONTANEOUS CASE WAS REPORTED BY A CONSUMER FROM GERMANY VIA SOCIAL MEDIA. THE REPORTER (CONSUMER) REPORTED USING TROJAN MAGNUM CONDOMS. AS PER THE REPORTER, "WE BOUGHT YOUR MAGNUMS AND OUT OF TWO 3 PACKS FOUR CONDOMS TORE THROUGH INTERCOURSE. I CAUGHT A STI (SEXUALLY TRANSMITTED INFECTION) DUE TO THAT INCIDENT." AS PER THE SOCIAL MEDIA CONVERSATION, THE REPORTER STATED, "I HAVE ALREADY BEEN AND NOW HAVE CHLAMYDIA DUE THOSE CONDOMS TORN". THE REPORTER FURTHER STATED, "I DEVELOPED SYMPTOMS SHORTLY AFTER USING THE PRODUCT. NO ADDITIONAL INFORMATION WAS AVAILABLE. MEDICAL HISTORY AND CONCOMITANT MEDICATION - UNKNOWN.
Patient problems: Sexually Transmitted Infection
MAUDE report 23677064 ↗InjuryAug 21, 2025Break; Break
ON AN UNSPECIFIED DATE, THE CONSUMER USED THE TROJAN MAGNUM CONDOMS DURING INTERCOURSE AND THE CONDOM BROKE. THE CONSUMER STATES " THEY USED MAGNUM, AND IT BROKE DURING INTERCOURSE". THE CONSUMER ALSO STATES "I NOW HAVE STDS. I WENT TO THE DOCTOR AND CONTACTED A LAWYER WHO WILL CONTACT YOU". THE ACTION TAKEN WITH TROJAN MAGNUM CONDOMS WAS NOT AVAILABLE. THE OUTCOME OF THE EVENTS BROKE AND DID NOT WORK WAS NOT AVAILABLE. THE OUTCOME OF THE EVENT SEXUALLY TRANSMITTED INFECTION WAS NOT AVAILABLE.
Patient problems: Sexually Transmitted Infection
MAUDE report 22857976 ↗
Other CONDOM devices
- 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
- 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.
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