Love and colleagues' results showed that the FDA tests for 13 types of drug residues, in contrast to inspection agencies in Europe and Japan that test for 34 and 27 drugs, respectively. This discrepancy suggests that seafood producers can use many drugs for which the U.S. does not screen. Based on the authors' findings of drug residues, it can be surmised that veterinary drugs are continuing to be used in aquaculture from developing countries, which can lead to adverse health consequences, including the development of antibiotic-resistant bacteria on fish farms and their spread in seafood products.
Imports to the U.S., E.U., Canada and Japan with the highest frequency of drug violations were shrimp or prawns, eel, crabs, catfish or pangasius, tilapia and salmon. Vietnam, China, Thailand, Indonesia, Taiwan, India, and Malaysia were identified as the exporters to the U.S., E.U., Canada and Japan with the most drug violations.
According to Love, "Consumers should be familiar with the country-of-origin and whether the animal was wild-caught or farm-raised." Love admits, "Fortunately, this information has been listed on all raw or lightly processed seafood products in grocery stores since 2005, following the Country of Origin Labeling (COOL) law."
"Imported seafood may carry risks in terms of food safety because the FDA does not have the resources to proactively and regularly inspect foreign facilities, and it relies on product testing as a last resort," said Love. To minimize the risks of seafood imports and to raise U.S. testing standards to match those of other countries, the authors recommend that the FDA budget be expanded to all
|Contact: Tim Parsons|
Johns Hopkins University Bloomberg School of Public Health