Food recall: Solbar Q Soy Protein Isolates. Item No. / Item Description: 22843 / Solbar Q 843 GMO, 22910 / Solbar Q 910 GMO, 22942…
Class I FDA enforcement event 65227. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Certain Soy-based products produced at the Ashdod Israel production facility have the potential to be contaminated with Salmonella
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Chs Inc started this food recall on 16 May 2013. The firm address in the FDA record is in Inver Grove Heights, MN. FDA put the recall in Class I. FDA event 65227 has 4 product records. The first FDA enforcement report date is 17 Jul 2013. The record gives the status Terminated, with the termination date 10 Mar 2015.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
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,…
Recalling firm
Chs Inc, Inver Grove Heights, MN.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
4 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1638-2013 | 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 | 1,671,960 kilograms | Class I | Terminated | 17 Jul 2013 |
| F-1639-2013 | Solcon Soy Protein Concentrates. Item No. / Item Description: 12110 / Solcon F GMO, 3112030 / Solcon F Soy Protein Concentrate, 12100 / Solcon GMO, and 3112002 / Solcon GMO Soy Protein Concentrate | 2,536,725 kilograms | Class II | Terminated | 17 Jul 2013 |
| F-1640-2013 | Solcon S Functional Soy Protein Concentrates. Item No. / Item Description: 3232212 / Solcon S 110 GMO, and 32211 / Solcon S110 GMO | 161,400 killograms | Class II | Terminated | 17 Jul 2013 |
| F-1641-2013 | 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,… | 651,225 kilograms | Class II | Terminated | 17 Jul 2013 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2013
- 546
- Share of these events in Class I
- 37%
- Product records in this event
- 4
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-1638-2013The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 65227. https://recallregister.com/fda/i/65227/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this 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,…
- What quantity of product is in FDA event 65227?
- The event has 4 product records. The first record gives this quantity:
1,671,960 kilograms
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2013 have the same class?
- 37% of the 546 food events that started in 2013 are in Class I.