Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin 00022600646143Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00022600646143), received between May 26, 2020 and Dec 8, 2021 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 8, 2021Adverse Event Without Identified Device or Use Problem

  AN (B)(6) REVIEW WAS RECEIVED FROM SOMEONE ALLEGING THAT HE HAS AIDS AND HAS ONLY ONE YEAR LEFT TO LIVE AFTER A SEXUAL ENCOUNTER WITH A WOMAN HE MET. THERE IS NO ACTUAL INDICATION OF A PRODUCT MALFUNCTION OR THAT THE PRODUCT WAS EVEN USED ALTHOUGH IT IS IMPLIED. IN THE ABSENCE OF CONFIRMATION, THIS EVENT IS REPORTABLE BASED ON THE ALLEGATION OF CONTRACTING AN STD/STI.

  Patient problems: Sexually Transmitted Infection

  MAUDE report 12961791 ↗
• InjuryMay 26, 2020Break; Product Quality Problem

  THE CONSUMER ALLEGES THAT ALL THREE CONDOMS IN THE BOX BROKE. THE CONDOMS BROKE NEAR THE TIP AND AROUND THE CIRCUMFERENCE DURING INTERCOURSE. HE BEGAN USING THE CONDOMS FROM THIS PARTICULAR BOX ON (B)(6) 2020 AND FINISHED USING ALL OF THE CONDOMS ON (B)(6) 2020. HE ALSO BELIEVES THAT HE CONTRACTED A URINARY TRACT INFECTION FROM THESE CONDOMS. HE FURTHER EXPLAINED THAT STARTING ON (B)(6) 2020, HE EXPERIENCED BURNING WITH URINATION. AS OF (B)(6) 2020 (WHEN HE CONTACTED US), HE IS STILL EXPERIENCING THESE SYMPTOMS. HE DID NOT SEEK MEDICAL ATTENTION.

  Patient problems: Urinary Tract Infection

  MAUDE report 10087806 ↗