PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MNCD 25LB BG, PROSANTE TSOYFLR 5P MNCD 50LB BG, PROSANTE TSOYF
Summary
The FDA issued a Class II for PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MNCD 25LB BG, PROSANTE 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-0789-2023
Action Date
2023-05-10
Status
Terminated
Category
food
Product Description
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
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 Affected: 4,858,300
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-0789-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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