Listeria monocytogenes is ubiquitous in the environment and in food process
ing plants. Consequently, foods are frequently contaminated. However, the o
ccurrence rate of listeriosis is only about five cases per million people p
er year. Listeriosis primarily strikes immunocompromised individuals, pregn
ant women and the elderly with a fatality rate of 20-25%. The FDA is in the
process of finishing a risk assessment that is being conducted as an initi
al step in reviewing its approach to maximizing the public protection from
foodborne L. monocytogenes. The risk assessment evaluated the presence and
quantitative levels of L. monocytogenes in 21 groups of ready-to-eat foods.
The potential growth of L. monocytogenes between retail point-of-sale, whe
re contamination data originated, and consumption was modelled. The frequen
cy and amount of consumption of these foods completed the data for the expo
sure assessment. For the hazard characterization or dose response part of t
he risk assessment, data from animal studies, virulence assays and epidemio
logical investigations were used to estimate the likelihood of illness for
different human groups from consuming different numbers of L. monocytogenes
. This risk assessment is a virtual review of current scientific knowledge.
Quantitative modelling provides greater insight than a qualitative review
and also indicates the uncertainty about our knowledge. The risk assessment
does not attempt to der ne an acceptable or tolerable level of L. monocyto
genes consumption or propose changes in regulations. These decisions are th
e responsibility of risk managers who consider additional factors such as f
ood preferences, technical feasibility and societal values when evaluating
regulatory policies.