PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, pape
Summary
The FDA issued a Class II for PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PRO by Cargill, Inc Corporate Headquarters. Reason: Products with a gluten free claim may contain gluten levels above 20 ppm..
Details
Source
Food Recall
External ID
F-0780-2023
Action Date
2023-05-10
Status
Terminated
Category
food
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
Lot/Code Info: 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
Quantity Affected: 977,000 lbs
Reason for Recall
Products with a gluten free claim may contain gluten levels above 20 ppm.
Distribution
Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-30
Company
Wayzata, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 65 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Cargill, Inc Corporate Headquarters has 24 FDA actions in our database, including 24 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Cargill, Inc Corporate Headquarters) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cargill, Inc Corporate Headquarters have FDA actions?
Cargill, Inc Corporate Headquarters has 24 FDA actions in our database, including 24 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0780-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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