Trojan Ecstasy Ultra Ribbed Lubricated Condom 00022600900238Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600900238), received between May 27, 2022 and May 27, 2022 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 27, 2022Break; Break

  THIS SPONTANEOUS REPORT (2022-CDW-00149, (B)(6)) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A MALE CONSUMER WHOSE CONDOM BROKE DURING THEIR INTERCOURSE AND GOT A RASH COINCIDENT WITH (B)(6) CONDOMS. THE CONSUMER MEDICAL HISTORY AND CONCOMITANT MEDICATIONS WERE NOT REPORTED. ON (B)(6) 2022 AN HOUR PRIOR TO THIS REPORT, THE CONSUMER APPLIED (B)(6) CONDOMS FOR INTERCOURSE WITH A MALE PARTNER. HE STATED THAT DURING INTERCOURSE, THE CONDOM BROKE AND WAS NOT SURE IF HE HAD BEEN IN DIRECT CONTACT WITH THE PARTNER. HE INDICATED THAT HE HAD GOTTEN A RASH. HE DID NOT KNOW THE HISTORY OF HIS PARTNER. NO ADDITIONAL INFORMATION AVAILABLE. THE ACTION TAKEN WITH (B)(6) CONDOMS WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT CONDOM BROKE DURING THEIR INTERCOURSE WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT IN GETTING A RASH WAS UNKNOWN.

  Patient problems: Rash

  MAUDE report 14521310 ↗