Trojan Extended Pleasure Condom 00022600999393Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600999393), received between May 24, 2022 and May 24, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 24, 2022Material Fragmentation; Material Fragmentation

  THIS SPONTANEOUS REPORT (2022-CDW-00144, 007528235A) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER AND CONCERNS A PATIENT (AGE AND GENDER UNSPECIFIED) WHO WAS DIAGNOSED WITH AIDS AS COINCIDENTLY CONDOM RIPPED ((B)(6) CONDOMS). THE PATIENT'S MEDICAL HISTORY AND CONCOMITANT MEDICATIONS WERE NOT REPORTED. ON AN UNSPECIFIED DATE, THE PATIENT INITIATED (B)(6) CONDOMS FOR UNKNOWN INDICATION. THE PATIENT STATED CONDOM RIPPED AND PATIENT WAS DIAGNOSED WITH AIDS (ACQUIRED IMMUNODEFICIENCY SYNDROME). NO PRODUCT SAMPLE FOR PLEASURE LUBRICATED CONDOMS RECEIVED. NO ADDITIONAL INFORMATION WAS AVAILABLE. ACTION TAKEN WITH (B)(6) CONDOMS NOT APPLICABLE. THE OUTCOME OF THE EVENT I JUST GOT DIAGNOSED WITH AIDS WAS UNKNOWN. THE OUTCOME OF THE EVENT CONDOM RIPPED WAS NOT APPLICABLE.

  Patient problems: Viral Infection

  MAUDE report 14487004 ↗