RecallHawk
Class II Recall

PROSANTE TSOYFLR 7P MNCD 25LB BG/40P, PROSANTE TSOYFLR 7P MNCD 50LB BG, 25 lb and 50lb paper bags

Cargill, Inc Corporate Headquarters

Summary

The FDA issued a Class II for PROSANTE TSOYFLR 7P MNCD 25LB BG/40P, PROSANTE TSOYFLR 7P MNCD 50LB BG, 25 lb an 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-0798-2023

Action Date

2023-05-10

Status

Terminated

Category

food

Product Description

PROSANTE TSOYFLR 7P MNCD 25LB BG/40P, PROSANTE TSOYFLR 7P MNCD 50LB BG, 25 lb and 50lb paper bags

Lot/Code Info: 100001411-02323CHXEA 100001411-03823CHXEA 100001411-04023CHXEA 100001411-07123CHXEA 100001411-07223CHXEA 100001411-28322CHXEA 100001411-30422CHXEA 100001411-30522CHXEA 100001411-32122CHXEA 100001411-32222CHXEA 100001411-33222CHXEA 100001411-34622CHXEA 100001411-34722CHXEA 100001412-32122CHXEA

Quantity Affected: 641,675 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

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-0798-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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