Safety Alert for Durex Prolong Condom , Durex Invisible Ultra Thin Condom, Durex Tropical Exciting Mix of Flavors and Colors Ultra Fine Lubricated Latex Condom

According to Food and Drug Administration Philippines, this safety alert involved a device in Philippines that was produced by manufacturer #17352.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Event Number
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    Data from the Philippines is current through 2019. All of the data comes from the Food and Drug Administration Philippines, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Philippines.
  • Extra notes in the data
  • Reason
    Fda advisory no. 2018-272 public health warning against the purchase and use of the following unregistered medical device products: durex prolong condom durex invisible ultra thin condom durex tropical exciting mix of flavors and colors ultra fine lubricated latex condom the food and drug administration (fda) advises the public against the purchase and use of the following unregistered medical device products: fda post-marketing surveillance (pms) activities have verified that the abovementioned medical device products have not gone through the registration process of the agency and have not been issued with proper authorization in the form of certificate of product registration (cpr). pursuant to republic act 9711, otherwise known as the “food and drug administration act of 2009”, the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promotion, advertising or sponsorship of health products without the proper authorization from fda is prohibited. accordingly, since these unregistered medical device products have not gone through evaluation and testing process of the fda, the agency cannot guarantee its quality and safety. the use of such violative products may pose potential health hazards to the consuming public. in light of the above, the public is advised not to purchase the aforementioned violative products and to be vigilant against medical device that might not be duly registered with fda. always check if a medical device product has been registered with the fda before purchasing it by making use of the embedded search feature of the fda website accessible at www.Fda.Gov.Ph.  all concerned establishments and/or entities are warned not to distribute the above-identified violative medical device products until they have already been covered by the appropriate authorization, otherwise, regulatory actions and sanctions shall be strictly pursued. all local government units (lgus) and law enforcement agencies (leas) are requested to ensure that this product is not sold or made available in their localities or areas of jurisdiction.  for more information and inquiries, please e-mail us at this email address is being protected from spambots. you need javascript enabled to view it. , or call us at the center for device regulation, radiation health and research (cdrrhr) hotline (02) 857-1900 local 8301. dissemination of the information to all concerned is requested.     attachments: fda advisory no. 2018-272.Pdf.