FDA News Digest for August 19, 2002

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FDA News Digest
August 19, 2002

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FDA's Top Official Issues Statement on Metabolife

FDA Deputy Commissioner Dr. Lester M Crawford says FDA has asked the Justice
Department to pursue a criminal investigation of Metabolife regarding
possible false statements made to FDA about the existence of adverse event
reports related to the company's products.
http://www.fda.gov/bbs/topics/NEWS/2002/NEW00828.html
________________________________________________________________

Tissue-Processing Company Ordered to Recall Materials

FDA has ordered Georgia-based Cryolife Inc. to recall distributed human
tissue processed from Oct. 3, 2001 to the present.  FDA is taking this
action because the agency has determined that Cryolife cannot ensure that
the human tissue it processes for transplantation is free from fungal and
bacterial contaminants.
http://www.fda.gov/bbs/topics/NEWS/2002/NEW00827.html
________________________________________________________________

Public Should Avoid Chinese Diet Pills With Fenfluramine

Following reports from Japan of sickness and death associated with certain
Chinese weight-loss products that contain fenfluramine, FDA has warned
consumers to avoid these products.
http://www.fda.gov/bbs/topics/NEWS/2002/NEW00826.html
________________________________________________________________

Mammography Advisory Committee to Meet Aug. 26

FDA's National Mammography Quality Assurance Advisory Committee will have a
public meeting Aug. 26 in Gaithersburg, Md.  The agenda includes discussion
of potential new applications of full-field digital mammography and changes
to compliance guidance for the Mammography Quality Standards Act.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfAdvisory/details.cfm?mtg
=346
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