Published in Hepatitis Weekly, October 19th, 1998
Shays claimed a series of delays has given the corporate entities involved time to prepare for a FDA look-back which would identify donors infected with the virus who gave blood prior to July 1992. The FDA would then notify recipients of this potentially tainted blood about their risk of acquiring hepatitis C.
According to the CNN report, by Louise Schiavone, "the head of the FDA's...
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