Contaminants and Natural Toxicants
Subcommittee Meeting
Enterobacter
sakazakii Contamination in Powdered Infant
Formula
March 18-19, 2003
8:00 – 8:30 Welcome, Introduction and Charges – Christine J. Taylor, FDA
8:30 – 8:45 Administrative Issues - Jeanne Latham, FDA
8:45 – 9:15 Remarks by Chairpersons
9:15 – 3:45 Presentations by Guest Speakers
9:15 – 9:45 Tennessee outbreak investigation - Matthew Kuehnert, CDC
9:45 – 10:15 Other relevant investigations - Karl Klontz, FDA
10:15 – 10:30 Break
10:30 – 11:00 How individuals respond/Long term, chronic consequences – John Alexander, FDA
11:00 – 11:30 Questions to speakers
11:30 – 12:30 Lunch
12:30 – 1:00 General Microbiology, e.g., ecology, pathogenicity,
subtyping, etc.
Maria Nazarowec-White, Canada
1:00 – 1:30 Preliminary Subcommittee Discussion on Clinical Presentations
1:30 – 2:00 Microbial detection, clinical and food - Don Burr, FDA
2:00 – 2:30 Resistance – Thermal and other - Robert Buchanan, FDA
2:30 – 2:45 Break
2:45 – 3:15 Manufacturing process, microbial standards, summary of FDA field survey - Don Zink, FDA
3:15 – 3:45 Current marketing and use of powdered infant formula - Sue Ann Anderson, FDA
3:45 – 4:00 Questions to speakers
4:00 – 5:00 Public
Comment
5:00 – 6:00 Preliminary Discussion by Subcommittee
March 19
8:30 – 8:45 Opening Remarks
8:45 – 11:30 Subcommittee Discussion of Issues
10:00 - 10:15 Break
11:30 – 12:30 Lunch
12:30 – 3:00 Subcommittee Concluding Deliberations, Recommendations and Response to Charges