Trojan UltraFit Bare Feel 00022600001423Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600001423), received between Jan 19, 2022 and Jan 19, 2022 — classified as 1 injury.

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

• InjuryJan 19, 2022Output Problem

  THE CONSUMER CONTACTED VIA (B)(6) TO ALLEGE THAT ALTHOUGH HE BOUGHT LARGE SIZE TROJAN PLUS ULTRA FIT LUBRICATED CONDOMS, HE COULD TELL THEY WERE TOO TIGHT. FURTHER, HE ALLEGES THAT WHILE ENGAGING IN INTERCOURSE, HE COULDN'T FEEL HIS PENIS AND THAT WHEN HE PULLED OUT HIS PENIS WAS BLUE. HE ADDITIONALLY ALLEGES THAT HE HAD TO GO TO THE EMERGENCY ROOM TO HAVE THEM REMOVE THE CONDOM. THE CONSUMER DID NOT RESPOND TO A REQUEST FOR HIM TO SEND US A DIRECT MESSAGE FOR MORE INFORMATION ABOUT HIS EXPERIENCE. IN THE ABSENCE OF CONFIRMATION AND/OR MEDICAL RECORDS TO SUBSTANTIATE THE EXPERIENCE, THIS COMPLAINT WILL BE REPORTED CONSERVATIVELY BASED ON THE REPORTED ADVERSE EVENT.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 13290912 ↗