RecallWatchUSA

Home / Recalls / Medical Devices

Reckitt Benckiser LLC recalls Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00 Product Us

Recalled October 3, 2018 · FDA recall Z-3241-2018 · Reckitt Benckiser

Hazard
The products failed the filed specification of 1.0kPa for Burst Pressure. · FDA Class II
Units
487980 condoms
Sold at
US Nationwide.

Description

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

Product
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).
Manufacturer(s)
Reckitt Benckiser LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Reckitt Benckiser LLC recalls Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00 Product Us | RecallWatchUSA