Class II Recall

PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANTE TVGPTN 10B MNCD 50LB BG, PROSANTE TVGP

Summary

The FDA issued a Class II for PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANT 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-0785-2023

Action Date

2023-05-10

Status

Terminated

Product Description

PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANTE TVGPTN 10B MNCD 50LB BG, PROSANTE TVGPTN 10B MNCD 50LB BG 21/P; distributed in bulk tote and paper bags

Lot/Code Info: 100001356-00223CHXEA 100001356-00323CHXEA 100001356-01023CHXEA 100001356-01123CHXEA 100001356-01223CHXEA 100001356-01323CHXEA 100001356-03223CHXEA 100001356-04523CHXEA 100001356-04623CHXEA 100001356-04723CHXEA 100001356-05823CHXEA 100001356-28422CHXEA 100001356-28522CHXEA 100001356-28622CHXEA 100001356-30722CHXEA 100001356-31822CHXEA 100001356-31922CHXEA 100001356-33422CHXEA 100001356-33522CHXEA 100001356-33622CHXEA 100001356-34922CHXEA 100001361-01123CHXTA 100001361-01223CHXTA 100001361-04423CHXTA 100001364-00323CHXEA 100001364-00423CHXEA 100001364-00523CHXEA 100001364-00623CHXEA 100001364-02523CHXEA 100001364-02623CHXEA 100001364-03323CHXEA 100001364-27822CHXEA 100001364-27922CHXEA 100001364-28122CHXEA 100001364-29822CHXEA 100001364-29922CHXEA 100001364-30022CHXEA 100001364-30122CHXEA 100001364-30822CHXEA 100001364-32222CHXEA 100001364-32422CHXEA 100001364-32522CHXEA 100001364-32622CHXEA 100001364-32722CHXEA 100001364-35522CHXEA 100001364-35622CHXEA 100001364-36122CHXEA 100001364-36222CHXEA 100001364-36322CHXEA 130012781-00323CHXEA 130012781-03223CHXEA 130012781-05123CHXEA 130012781-29722CHXEA 130012781-29822CHXEA 130012781-32522CHXEA

Quantity Affected: 4,636,250 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

Cargill, Inc Corporate Headquarters

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-0785-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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