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DUREX RealFeel 20 ct condoms (2018-12-26)

Starting date:
December 26, 2018
Posting date:
December 27, 2018
Type of communication:
Medical Device Recall
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Medical Devices
General Public, Healthcare Professionals, Hospitals
Identification number:

  Affected products

DUREX RealFeel 20 ct condoms

A similar recall was initiated for DUREX Real Feel Extra Lubricated 10ct condoms on July 30, 2018.


Following observation of variable burst pressure performance of Polyisoprene Condoms manufactured during 2017, RB conducted an internal investigation and identified that a specific batch (1000356816) of DUREX RealFeel® 20 ct condoms distributed in Canada is not expected to meet the registered burst pressure specification at end of shelf-life. As a cautionary measure, RB Health (Canada) Inc. is initiating a consumer level recall.  

Affected products

DUREX RealFeel 20 ct condoms

Lot or serial number


Model or catalog number

97177 (20 COUNT)

Reckitt Benckiser (Canada) Inc
1680 Tech Avenue, Unit 2
Mississauga, Ontario
L4W 5S9