Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Durex Real Feel Polyisoprene Condoms Recalled by Reckitt Benckiser LLC Due to The products failed the filed specification of 1.0kPa...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Reckitt Benckiser LLC directly.
Affected Products
Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00 Product Usage: The Durex Synthetic polyisoprene male condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted disease).
Quantity: 487980 condoms
Why Was This Recalled?
The products failed the filed specification of 1.0kPa for Burst Pressure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Reckitt Benckiser LLC
Reckitt Benckiser LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report