Trojan™ Premium Latex Condoms Her Pleasure™ Sensations 00022600973201Recalls & reported problems
Church & Dwight CO., Inc. · For Contraception Plus STI Protection · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Dec 26, 2025Class IIOpen, Classified
Potential exposure of rodents and rodent activity in the distribution center.
Z-1181-2026 · Root cause: Storage · Recall details · FDA record ↗
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 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
- 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page