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Cargill, Inc Corporate Headquarters Recall: The firm was notified that foreign material was in the product.

United States

TerminatedClass II

Company
Cargill, Inc Corporate Headquarters
Product
Marigold, INC. Granulated Cane Sugar Net Weight: 2000#
Recall date
January 12, 2020
Terminated
February 24, 2022
Source
FDA

Reason for recall

The firm was notified that foreign material was in the product.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Marigold, INC. Granulated Cane Sugar Net Weight: 2000# Not published in this source record 93/2000# tote Seal #: 3205154 Lot #: AB20A071B Item ID: GRSCATT2K Production Date: 01/07/2020 Batch codes: AB19L263B, AB19L273B & AB19L271B

Distribution

  • Product was shipped to Georgia

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0589-2020
Event ID
84701
Status
Terminated
Classification
Class II
Company
Cargill, Inc Corporate Headquarters
Product description
Marigold, INC. Granulated Cane Sugar Net Weight: 2000#
Quantity
93/2000# tote
Reason
The firm was notified that foreign material was in the product.
Recall initiation date
January 12, 2020
Report date
February 12, 2020
Classification date
Not published in this source record
Termination date
February 24, 2022
Distribution pattern
Product was shipped to Georgia
UPC, lot, and code information
Seal #: 3205154 Lot #: AB20A071B Item ID: GRSCATT2K Production Date: 01/07/2020 Batch codes: AB19L263B, AB19L273B & AB19L271B
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Cargill, Inc Corporate Headquarters

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Where this information comes from

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

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

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

Retrieved by Public Health Trace:

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.

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.