Reported Oct 3, 2018 · Terminated

Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00 Product…

Reckitt Benckiser LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Reckitt Benckiser LLC · 399 Interpace Pkwy · Parsippany, NJ · 07054-1133

Is this the product you have?

    • Durex Real Feel Polyisoprene Condoms
    • 10 count and 24 count
    • SKU Numbers 02340-89456-14
  • and 02340-89457-00 Product UsageThe Durex Synthetic polyisoprene male condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted disease)
Lot codes and dates
  • Batch Numbers
    • 1000427177
    • 1000408620
    • 1000430764
Amount recalled
487980 condoms

Where it was sold

  • Nationwide

Why it was recalled

The products failed the filed specification of 1.0kPa for Burst Pressure.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Reckitt Benckiser LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 5, 2020 · Data as of Sep 19, 5:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.