Solbar Q Soy Protein Isolates. Item No. / Item Description: 22843 / Solbar Q 843 GMO, 22910 / Solbar Q 910 GMO, 22942 / Solbar Q 842 GMO, 22943 / Solbar Q 842 NGMO, 3323912 / Solbar Q 910, 3323920 / Solbar Q 920, 3323932 / Solbar Q 842, and 3323973 / Solbar Q 842 IP

Chs INC recalled Solbar Q Soy Protein Isolates. in a Class I action — the FDA's most serious tier, reserved for products with a reasonable probability of causing serious health consequences or death on May 16, 2013.

The recall was triggered by possible Salmonella contamination: "Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella" Salmonella is one of the most common causes of U.S. foodborne illness, with symptoms that typically appear within six hours to six days of exposure.

Distribution was broad: the FDA record describes it as "Nationwide. Product was shipped from the Israel facility to the following countries. This product did not come into the U.S. before shipment to the following countries: Canada, Australia, Belgium, Brazil, Bulgaria, Chile, Columbia, Costa Rica, Czech Republic, Denmark, Finland, France, Germany, Greece, Guatemala, Hungary, India, Israel, Italy, Japan, Lithuania, Mauritius, Mexico, Netherlands, New Zealand, Panama, Poland, Portugal, Romania, Russia, Serbia, Slovakia, Slovenia, South Africa, South Korea, Spain, Taiwan, Thailand, United Kingdom, Uruguay, and Vietnam," which places this among the wider-reach recalls on the site. Consumers across the affected area should check product on hand. The recalling firm is based in Inver Grove Heights, MN. The recall covers 1,671,960 kilograms of product. The FDA has Terminated this recall (first reported Jul 17, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.