Severity
Critical
FDA Food recall · Reported July 17, 2013
Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella
Chs Inc recalled Solbar Q Soy Protein Isolates. Item No. / Item Description: 22843 / Solbar Q 843 GMO, 2… - a critical-severity action.
Solbar Q Soy Protein Isolates. Item No. / Item Description: 22843 / Solbar Q 843 GMO, 2… was recalled by Chs Inc in July 17, 2013. Reason: Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contami…. Check the official notice for the remedy. Verify recall #F-1638-2013 with the FDA Food before acting.
The recall
Chs Inc issued this critical-severity FDA Food recall-Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contami….
Sourced from official FDA Food enforcement records. Verify recall #F-1638-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1638-2013) was formally reported on July 17, 2013, with the manufacturer initiating the action on May 16, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Chs Inc is listed as the recalling firm, operating out of Inver Grove Heights, MN. Federal records list the affected scope as 1,671,960 kilograms.
The documented reason for this recall is: Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella Distribution data in the federal record shows the product reached: 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, C…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
1,671,960 kilograms
Related Recalls
6
6 from same agency
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
Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1638-2013 |
| Date reported | July 17, 2013 |
| Date initiated | May 16, 2013 |
| Recalling firm | Chs Inc |
| Firm location | Inver Grove Heights, MN |
| Affected scope | 1,671,960 kilograms |
| Distribution | 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, Cost… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 17, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.