Trojan™ Premium Latex Condoms Pleasures Fire & Ice™ 00022600960034Recalls & reported problems
Church & Dwight CO., Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600960034), received between Nov 4, 2020 and Nov 4, 2020 — classified as 1 malfunction.
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
Device problems
- Break1
Patient problems
- Herpes1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 4, 2020Break
THE CONSUMER STATED THAT HE PUT ON TWO CONDOMS AT ONE TIME AND HAD INTERCOURSE. THE OUTER CONDOM TORE AT THE TOP. HE FURTHER STATED THAT THE NEXT DAY IT BURNED WHEN HE URINATED. THE CONSUMER WENT TO THE EMERGENCY ROOM WHERE HE ALLEGES THAT HE TESTED POSITIVE FOR GENITAL HERPES. IN THE EMERGENCY ROOM, THEY RECOMMENDED AN OVER THE COUNTER CREAM AT (B)(4). HE STILL HAS ONGOING SYMPTOMS. WE DON'T HAVE MEDICAL RECORDS TO CONFIRM THIS DIAGNOSIS. ALSO, THERE WAS NO MENTION OF THE SECOND CONDOM BREAKING; HOWEVER, WE DON'T HAVE ADDITIONAL RECORDS TO CONFIRM THIS INFORMATION.
Patient problems: Herpes
MAUDE report 10788574 ↗
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 BareSkin™ Value Pack 00022600998532Church & Dwight CO., Inc. · CONDOM3 reports
- Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin 00022600646143Church & Dwight CO., Inc. · 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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