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Trojan™ Premium Latex Condoms BareSkin™ Value Pack 00022600998532Recalls & reported problems

Church & Dwight CO., Inc. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00022600998532), received between Oct 22, 2020 and Mar 17, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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

Device problems

  • Break2
  • Material Puncture/Hole1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Insufficient Information1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 17, 2022Break

    AN AMAZON REVIEW WAS RECEIVED FROM A CONSUMER STATING THAT MULTIPLE PACKS OF TROJAN BARESKIN CONDOMS HAVE BROKEN. THE CONSUMER ALLEGES THAT PLAN B WAS PURCHASED IN ADDITION TO GOING FOR STI TESTING. IN THE ABSENCE OF CONFIRMATION, THIS COMPLAINT WILL BE CONSERVATIVELY REPORTED BASED ON THE ALLEGATION OF A PRODUCT MALFUNCTION.

    Patient problems: Insufficient Information

    MAUDE report 13791101 ↗
  • MalfunctionAug 4, 2021Break

    THE CONSUMER ALLEGES THAT TWO CONDOMS FROM THE SAME BOX OF TROJAN BARESKIN CONDOMS HAD BROKEN. THE CONDOMS BROKE ON THE BODY OF THE CONDOMS DOWN THE SIDES DURING INTERCOURSE. THE CONSUMER ALSO STATED THAT SHE HAD SOUGHT MEDICAL ATTENTION FROM PLANNED PARENTHOOD AND HAD AN HIV AND OTHER TESTS DONE. SHE FURTHER STATED THE HIV TEST WAS NEGATIVE. SHE WAS TOLD BY PLANNED PARENTHOOD THAT THE OTHER RESULTS WOULD TAKE 7-10 BUSINESS DAYS TO BE AVAILABLE. SHE SAID THAT PLANNED PARENTHOOD STATED THAT IF SHE HAD NOT HEARD FROM THEM, THAT NO NEWS WAS GOOD NEWS. THIS PRODUCT WOULD NOT BE EXPECTED TO BE ASSOCIATED WITH STDS; HOWEVER, IN THE ABSENCE OF MEDICAL RECORDS, WE CANNOT ELIMINATE THE POTENTIAL INVOLVEMENT OF THE CONDOM. THIS CONTACT WILL BE REPORTED CONSERVATIVELY, AS THIS CAN BE A SERIOUS INJURY.

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

    MAUDE report 12274227 ↗
  • MalfunctionOct 22, 2020Material Puncture/Hole

    THE CONSUMER STATES THAT HE PURCHASED A 24 PACK OF TROJAN BARESKIN CONDOMS. HE ALLEGES THAT OUT OF THE FIRST FIVE CONDOMS, THREE RIPPED. HE FURTHER STATED THAT HE HAS (B)(6). THIS IS BEING REPORTED AS A MALFUNCTION WITH A RISK OF EXPOSURE TO A STI.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10722165 ↗

Other CONDOM devices

All CONDOM devices →

Sources and updates

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