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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 1 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. 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

All CONDOM devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page