Class IITerminated in FDA datasetRecall initiated Mar 30, 2023

Prosante Tsoyflr 3018p Flk 50lb Bg, Prosante Tsoyflr 3018p Flk 50lb Bg 18/P, Prosante Tsoyflr…

Recalling firm: Cargill, Inc Corporate Headquarters

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 8, 2023.

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Compare the exact product and package details with the label you have.

ProductPROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
Package size50LB

FDA code information

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

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Full FDA record and distribution details

Original product description

PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag

Original FDA recall reason

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

Recall details

Recall number
F-0780-2023
Event ID
92013
FDA status
Terminated
Initiated
Mar 30, 2023
Reported
May 10, 2023
Classified
May 1, 2023
Terminated
Jun 8, 2023
Quantity
977,000 lbs
Location
Wayzata, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

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

FDA source record · F-0780-2023

Data updated September 16, 2026. View official FDA data ↗

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