Recall record at a glance
| Official record | F-1641-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Chs Inc. |
| Report date | Jul 17, 2013 |
| Recall initiation date | May 16, 2013 |
| Quantity | 651,225 kilograms |
| Location | Inver Grove Heights, MN, United States |
Official product description
Contex - Textured Soy Protein Concentrates Item No. / Item Description: 3411112 / Contex 120 Textured Soy Protein, 3411124 / Contex 25 Textured Soy Protein, 3411129 / Contex 31 CL Textured Soy Protein, 3411142 / Contex 120CL IP Textured Soy Protein, 3411144 / Contex 240 Textured Soy Protein, 3411161 / Contex 25 CLH, 51026 / Contex 25 Textured NGMO Soy Protein, 52031 / Contex 31 GMO Textured Soy Protein, 52032 / Contex 31 CL GMO Textured Soy Protein, 52034 / Contex 31PV GMO Textured Soy Protein, 52035 / Contex 31NP GMO Textured Soy Protein, 52121 / Contex 120CL IP Textured Soy Protein, and 52248 / Contex 240CL GMO Textured Soy Protein.
Why the product was recalled
Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella
Distribution information
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
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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