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FDA News & Notes - Week of July 25, 2011
Date:7/25/2011

seeking to expedite notifications of human drug product recalls to the public. The agency will modify the drug product section of the Enforcement Report, published every Wednesday, to include actions that have been determined to be recalls, but that remain in the process of being classified as a Class I, II, or III action. Such recalls will be listed under the heading, "Recalls Pending Classification: DRUGS." They will be reposted with their classification once that determination has been made. Send comments or suggestions to RecallPilot@fda.hhs.gov.
Press Office Contact: Shelly Burgess, 301-796-4651, shelly.burgess@fda.hhs.gov

Analysis of Premarket Review Times Under the 510(k) Program at Center for Devices and Radiological Health.
Press Office Contact: Karen Riley, 301-796-4674, karen.riley@fda.hhs.gov

Guidance for Industry and FDA Staff - Establishing the Performance Characteristics of In Vitro Diagnostic Devices for the Detection or Detection and Differentiation of Influenza Viruses
Press Office Contact: Erica Jefferson, 301-796-4988, erica.jefferson@fda.hhs.gov

FDA Office of Public Affairs Contact Information:
Call or email FDA Office of Public Affairs, 301-796-4540, fdaopa@fda.hhs.gov
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