Summary
The FDA issued a Class II for PROSANTE TVGPTN 12BF MNCD 50LB BG/36P, paper bag 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-0800-2023
Action Date
2023-05-10
Status
Terminated
Category
food
Product Description
PROSANTE TVGPTN 12BF MNCD 50LB BG/36P, paper bag
Lot/Code Info: 110025739-36022CHXEA
Quantity Affected: 2,436,000 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-0800-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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