PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MNCD 25LB BG, PROSANTE TSOYFLR…
Cargill, Inc Corporate Headquarters recalled this product and the FDA reported the enforcement action on 10 May 2023 as Class II. The recall was initiated by the firm. Products with a gluten free claim may contain gluten levels above 20 ppm.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MNCD 25LB BG, PROSANTE TSOYFLR 5P MNCD 50LB BG, PROSANTE TSOYFLR 5P MNCD 800LB TT; distributed paper bags and bulk totes
- Reason for recall
- Products with a gluten free claim may contain gluten levels above 20 ppm.
- Recalling firm
- Cargill, Inc Corporate Headquarters
- Firm location
- Wayzata, Minnesota, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0789-2023
- Quantity
- 4,858,300
- Distribution
- Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
- Initiated
- 30 March 2023
- Reported by FDA
- 10 May 2023
- Terminated
- 8 June 2023
- Firm notified by
- Product codes
- 100001404-00923CHXTA 100001404-01023CHXTA 100001404-01123CHXTA 100001404-04523CHXTA 100001404-04623CHXTA 100001404-04723CHXTA 100001404-06523CHXTA 100001404-06623CHXTA 100001404-06723CHXTA 100001404-28322CHXTA 100001404-28422CHXTA 100001404-28522CHXTA 100001404-30422CHXTA 100001404-30522CHXTA 100001404-30622CHXTA 100001404-31822CHXTA 100001404-31922CHXTA 100001404-32022CHXTA 100001404-33222CHXTA 100001404-33322CHXTA 100001404-33422CHXTA 100001404-34622CHXTA 100001404-34722CHXTA 100001404-34822CHXTA 100001406-01623CHXEA 100001406-01723CHXEA 100001406-03923CHXEA 100001406-07523CHXEA 100001406-08623CHXEA 100001406-29222CHXEA 100001406-30522CHXEA 100001406-30622CHXEA 100001406-30722CHXEA 100001406-30822CHXEA 100001406-34022CHXEA 100001406-34122CHXEA 100001406-34222CHXEA 100001406-35422CHXEA 100001406-35522CHXEA 100001406-35622CHXEA 130012710-05223CHXEA 130012710-05323CHXEA 130012710-06523CHXEA 130012710-06623CHXEA 130012710-06723CHXEA 130012710-06823CHXEA 130012710-08723CHXEA 130012710-08823CHXEA 130015053-01823CHXEA 130015053-01923CHXEA 130015053-29222CHXEA 130015053-29422CHXEA 130015053-30422CHXEA 130015053-30822CHXEA 130015053-31322CHXEA 130015053-31422CHXEA
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 22 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 22 separate recalls, which almost every published figure does, overstates it by a factor of 22. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 22 of them.
- The recall ran for 2 months, from 30 March 2023 to termination on 8 June 2023. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 6 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Other records from Cargill, Inc Corporate Headquarters
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 29 other records name this firm.
All 30 records for Cargill, Inc Corporate Headquarters
All 2023 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.