Durex Real Feel Polyisoprene condoms (10/24 count) with specific SKUs and batch numbers were recalled due to failing burst pressure tests. Consumers should check their product details and contact the manufacturer for guidance.
The products failed the filed specification of 1.0kPa for Burst Pressure.
Durex Real Feel Polyisoprene condoms (10-count and 24-count packs) were recalled because they failed burst pressure tests. This could lead to condom failure during use, potentially causing injury or pregnancy.
The condoms failed to meet the required burst pressure of 1.0kPa, meaning they could rupture under normal use conditions. This increases the risk of unintended pregnancy or STI transmission if the condom breaks during sexual activity.
Anyone who owns or uses Durex Real Feel Polyisoprene condoms with the listed SKUs and batch numbers. Men who use these condoms for contraception or STI prevention are most at risk.
Check for SKU numbers 02340-89456-14 or 02340-89457-00 and batch numbers 1000427177, 1000408620, or 1000430764 on the product packaging.
Look for SKU numbers 02340-89456-14 or 02340-89457-00 and batch numbers 1000427177, 1000408620, or 1000430764 on the condom packaging.
The condoms failed the required burst pressure test of 1.0kPa, which could lead to rupture during use.
Check for SKU numbers 02340-89456-14 or 02340-89457-00 and batch numbers 1000427177, 1000408620, or 1000430764 on the product packaging.
The recall indicates a potential risk of rupture, but the remedy is not specified. Consumers should check their product details and contact the manufacturer for guidance.
We’ve drafted a message you can send Durex to request your refund or repair — edit it as you like.
Subject: Recall Z-3241-2018 — Durex Durex Hello, I own a Durex that is covered by recall Z-3241-2018 from Durex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
