FDA recall record
PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
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 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
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 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
Code information listed by FDA
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
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: 977,000 lbs
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.