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FDA source record Class II Terminated

Cargill Trisodium Citrate Dihydrate packaged in 50 lb. paper bags and 2,000 lb. supersacks. Product item ids: 1. SKU 100002299, TSC DIHYD FN 50LB BG 6132-04-3 KH FC 2. SKU 10...

Recall Date: 2023-06-23 Recalling Firm: Cargill, Inc Corporate Headquarters Record Ref: F-1222-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Cargill Trisodium Citrate Dihydrate packaged in 50 lb. paper bags and 2,000 lb. supersacks. Product item ids: 1. SKU 100002299, TSC DIHYD FN 50LB BG 6132-04-3 KH FC 2. SKU 10... and names Cargill, Inc Corporate Headquarters as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Cargill, Inc Corporate Headquarters
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2023-06-23
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Product Description & Identification

Cargill Trisodium Citrate Dihydrate packaged in 50 lb. paper bags and 2,000 lb. supersacks. Product item ids: 1. SKU 100002299, TSC DIHYD FN 50LB BG 6132-04-3 KH FC 2. SKU 100105400, TSC DIHYD FN 2000LB RED HNDL SS KH 3. SKU 100106066, TSC DIHYD FN 2000LB RED HNDL SS KH FCC 4. SKU 100105370, TSC DIHYD GNLR 50LB BG KH FCC 5. SKU 100105374, TSC DIHYD GNLR 2000LB RED HNDL SS KH FCC

Reason for Recall / Hazard Identified

Potential for foreign material (metal).

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributors and manufactures in AZ, CA, DE, IL, LA, MI, MN, MO, OH, PA, TX, VA, WI and Canada.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1222-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record