Recall record at a glance
| Official record | F-1222-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Cargill, Inc Corporate Headquarters |
| Report date | Jul 12, 2023 |
| Recall initiation date | Jun 23, 2023 |
| Quantity | 1,610,900 lbs |
| Location | Wayzata, MN, United States |
Official product description
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
Why the product was recalled
Potential for foreign material (metal).
Distribution information
Distributors and manufactures in AZ, CA, DE, IL, LA, MI, MN, MO, OH, PA, TX, VA, WI and Canada.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.