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
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms 00022600642039Church & Dwight CO., Inc. · CONDOM1 recall2 reports
- Trojan™ Premium Latex Condoms Stimulations Ultra Ribbed 00022600940500Church & Dwight CO., Inc. · CONDOM1 recall1 report
- Trojan™ Premium Latex Condoms Sensitivity Ultra Thin 00022600926207Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms Her Pleasure™ Sensations 00022600973201Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms ENZ™ Armor Spermicidal Lubricant 00022600931508Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ ENZ™ Latex Lubricated Condoms 00022600930501Church & Dwight CO., Inc. · CONDOM1 recall0 reports
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin 00022600646143Church & Dwight CO., Inc. · CONDOM2 reports
- DUREX Invisible CondomRB Health (us) LLC · CONDOM2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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