PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB…
Food recall F-0780-2023. Published in FDA’s Enforcement Report on May 10, 2023.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on May 10, 2023. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 977,000 lbs how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Products with a gluten free claim may contain gluten levels above 20 ppm.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
977,000 lbs, in FDA’s words.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
100001351-00323CHXEA 100001351-00423CHXEA 100001351-01023CHXEA 100001351-28422CHXEA 110023777-00223CHXEA 110023777-00523CHXEA 110023777-00623CHXEA 110023777-01123CHXEA 110023777-01323CHXEA 110023777-03123CHXEA 110023777-03223CHXEA…
Every code shown here, 986 characters
100001351-00323CHXEA 100001351-00423CHXEA 100001351-01023CHXEA 100001351-28422CHXEA 110023777-00223CHXEA 110023777-00523CHXEA 110023777-00623CHXEA 110023777-01123CHXEA 110023777-01323CHXEA 110023777-03123CHXEA 110023777-03223CHXEA 110023777-03323CHXEA 110023777-05223CHXEA 110023777-05323CHXEA 110023777-05423CHXEA 110023777-05823CHXEA 110023777-05923CHXEA 110023777-06123CHXEA 110023777-27822CHXEA 110023777-27922CHXEA 110023777-28422CHXEA 110023777-28522CHXEA 110023777-28622CHXEA 110023777-28722CHXEA 110023777-29722CHXEA 110023777-29822CHXEA 110023777-30022CHXEA 110023777-32122CHXEA 110023777-33322CHXEA 110023777-33522CHXEA 110023777-36222CHXEA 110023777-36322CHXEA 110023777-36422CHXEA 100001351-31922CHXEA 100001351-32022CHXEA 100001351-33222CHXEA 100001351-33322CHXEA 110026502-00923CHXEA 110026502-03023CHXEA 110026502-07223CHXEA 110026502-28322CHXEA 110026502-29722CHXEA 110026502-29922CHXEA 110026502-31822CHXEA 110026502-31922CHXEA 110026502-33222CHXEA 110026502-36222CHXEA
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Mar 30, 2023.
- FDA classified it on May 1, 2023.
- FDA’s Enforcement Report published it on May 10, 2023.
- FDA terminated it on Jun 8, 2023.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Cargill, Inc Corporate Headquarters, of Wayzata, MN.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: E-Mail.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- Meat, poultry and egg products are recalled by USDA’s Food Safety and Inspection Service, not FDA, and its recalls aren’t here yet: see fsis.usda.gov.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Food recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.