FDA News Digest
July 30, 2007
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IN
THIS WEEK'S ISSUE
»
News
-- FDA Allows Restricted Use of Suspended Drug Zelnorm for Qualified Patients
-- Agency Report on Nanotechnology Outlines Scientific, Regulatory Challenges
» Safety Alerts/Recalls
» Congressional Testimony
» Question of the Week
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SAFETY
ALERTS/RECALLS
Also being
recalled:
products from the past 60 days, go to http://www.fda.gov/opacom/7alerts.html.
To access the RSS feed of FDA recalls information, go
to
http://www.fda.gov/oc/po/firmrecalls/rssRecalls.xml
[What is an RSS feed? See http://www.fda.gov/bbs/topics/news/newsfeeds.html.]
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CONGRESSIONAL TESTIMONY
July 24 -- FDA Assistant Commissioner for Food Protection David Acheson, M.D., appeared before the House Subcommittee on Emerging Threats, Cybersecurity, and Science and Technology
Subject: FDA food defense activities
http://www.fda.gov/ola/2007/foodsafety072407.html
To
view an archive of past testimony by FDA officials, go to
http://www.fda.gov/ola/listing.html
Does
a doctor always have to
refer a patient to a
mammography facility?
No. A patient can have a mammography exam and
receive the follow-up report without a doctor's referral (this is called a "self
referral"). Before the exam, however, verify that the facility accepts
self-referred patients because some facilities do not.
For more on mammography, see http://www.fda.gov/CDRH/MAMMOGRAPHY/
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