SILVER SPRING, Md., July 22 /PRNewswire-USNewswire/ -- Federal health officials are warning medical practitioners around the country not to use unapproved intrauterine devices (IUDs).
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In a July 22 letter, the Food and Drug Administration (FDA) reminds health professionals that using unapproved IUDs raises concerns about effectiveness and safety - as well as the potential for fraud and counterfeiting.
Learn what to do if you think you may have an unapproved IUD:
http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm219837.htm
Sign-up for e-mail notices of new FDA Consumer Updates at: https://service.govdelivery.com/service/subscribe.html?code=USFDA_9.
View the FDA Consumer Update RSS feed at: http://www.fda.gov/AboutFDA/ContactFDA/StayInformed/RSSFeeds/Consumers/rss.xml
FDA Consumer Updates may be posted and published elsewhere without permission. Please credit "FDA Consumer Health Information (www.fda.gov/consumer)" as the source. FDA values feedback on its consumer health information. Send questions, comments, or story ideas to: [email protected].
Contact: Jason Brodsky, 1-301-796-8234, [email protected], or Elaine Gansz Bobo, 1-301-796-7567, [email protected]
SOURCE U.S. Food and Drug Administration
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