Home/Recalls/CANADA-58703
Health CanadaType II

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

Published: December 27, 2018Recall ID: 58703Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

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

Additional Source Details

FieldValue
N I D58703
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/durex-realfeel-20-ct-condoms-2018-12-26
IssueMedical devices
Title DUREX RealFeel 20 ct condoms (2018-12-26)
Archived0
CategoryMedical devices
Last updated2018-12-27
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert