FDA Food Recalls

Recalls / Class II

Class IIF-0789-2023

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

Type
Food
Affected lot / code info
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
Quantity
4,858,300

Why it was recalled

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

Recalling firm

Firm
Cargill, Inc Corporate Headquarters
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
15407 McGinty Rd W, Wayzata, Minnesota 55391-2365

Distribution

Distribution pattern
Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom

Timeline

Recall initiated
2023-03-30
FDA classified
2023-05-01
Posted by FDA
2023-05-10
Terminated
2023-06-08
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-0789-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings.