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FDA recall record

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

Recall F-0789-2023Class IITerminatedMarch 30, 2023

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of June 8, 2023. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

Products with a gluten free claim may contain gluten levels above 20 ppm.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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

Code information listed by FDA

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

Distribution and firm information

Recalling firm listed by FDA: Cargill, Inc Corporate Headquarters

Firm location listed by FDA: Wayzata, MN, United States

Distribution reported by FDA: Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom

Product quantity listed by FDA: 4,858,300

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.