Trojan Supra™ Premium Condoms Non-Latex Bareskin™ 00022600902423Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600902423), received between Jan 5, 2023 and Jan 5, 2023 — classified as 1 malfunction.

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

• MalfunctionJan 5, 2023Device Slipped; Device Slipped

  THIS SPONTANEOUS REPORT (B)(4) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A FEMALE CONSUMER (AGE UNSPECIFIED) WHO FELT THE CONDOM LIKE PLASTIC, NOT COMFORTABLE, AND IT CAME OFF INSIDE HER WHILE USING TROJAN POLYURETHANE SUPRA BARESKIN CONDOMS. THE CONSUMER'S MEDICAL HISTORY AND THE CONCOMITANT MEDICATIONS WERE NOT REPORTED. ON AN UNSPECIFIED DATE, THE CONSUMER USED TROJAN POLYURETHANE SUPRA BARESKIN CONDOMS. WHILE USING IT, SHE FELT IT WAS LIKE PLASTIC AND NOT COMFORTABLE. SHE ALSO STATED THAT THE CONDOM CAME OFF INSIDE HER. HOWEVER, SHE CAUGHT IT IN TIME. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH TROJAN POLYURETHANE SUPRA BARESKIN CONDOMS WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT FELT THE CONDOM LIKE PLASTIC AND NOT COMFORTABLE WAS UNKNOWN. THE OUTCOME OF THE EVENT IT CAME OFF INSIDE HER WAS NOT APPLICABLE.

  Patient problems: Discomfort

  MAUDE report 16100686 ↗