Cargill, Inc Corporate Headquarters Recall: Products with a gluten free claim may contain gluten levels above 20 ppm.

🇺🇸 United States

1. March 30, 2023 - Recall initiated
2. May 10, 2023 - Reported by source
3. June 8, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0782-2023

Event ID

92013

Status

Terminated

Classification

Class II

Company

Cargill, Inc Corporate Headquarters

Product description

PROSANTE TVGPTN 3014B FLK 50LB BG, paper bag

Quantity

122,400 lbs

Reason

Products with a gluten free claim may contain gluten levels above 20 ppm.

Recall initiation date

March 30, 2023

Report date

May 10, 2023

Classification date

Not published in this source record

Termination date

June 8, 2023

Distribution pattern

Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom

UPC, lot, and code information

100001344-06623CHXEA 100001344-34622CHXEA

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 92013 with 10 other product entries in Public Health Trace.

Responsible company: Cargill, Inc Corporate Headquarters

Other recalls from Cargill, Inc Corporate Headquarters

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Official guidance and record verification

Public Health Trace does not provide medical advice. The information below explains how to interpret this record and links to relevant official government sources. Review the linked official source for the current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 8, 2023.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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