Cargill Trisodium Citrate Dihydrate packaged in 50 lb. paper bags and 2,000 lb.
Cargill, Inc Corporate Headquarters recalled this product and the FDA reported the enforcement action on 12 July 2023 as Class II. The recall was initiated by the firm. Potential for foreign material (metal).
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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
- Potential for foreign material (metal).
- Recalling firm
- Cargill, Inc Corporate Headquarters
- Firm location
- Wayzata, Minnesota, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1222-2023
- Quantity
- 1,610,900 lbs
- Distribution
- Distributors and manufactures in AZ, CA, DE, IL, LA, MI, MN, MO, OH, PA, TX, VA, WI and Canada.
- Initiated
- 23 June 2023
- Reported by FDA
- 12 July 2023
- Terminated
- 5 February 2025
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot IDs: 1. 31654856; 31966749; 31966836; 31967034; 32293580; 32293591; 32329808; 32342160 32490519; 32560914; 32786734; 32790606; 32832666; 32869093; 32869146; 32905026; 32981475; 32981483; 33042333; 33052549; 33059417; 33071513 2. 31781484; 31781485; 31828747; 31845892; 31857035; 31878282; 31904849; 31904851; 31966578; 32358277; 32376424; 32386329; 32406277; 32438147; 32406273; 32555414; 32641146; 32668049; 32704420; 32680600; 32766319; 32848927; 32869043; 32920483; 32937670; 32957630; 33111403; 33123226; 33123252; 33123255 3. 32008128; 32069695; 33200874; 33227563; 33256368 4. 31781482; 31966793; 31967013; 32046600; 32293609; 32342169; 32437279; 32437743; 32406272; 32464314; 32490553; 32560920; 32786755; 32790676; 32832672; 32869107; 32869157; 32905031; 32981500; 32981507; 33034261; 33059423; 33071522 5. 31781483; 31828744; 31845890; 31857031; 31878220; 31904863; 31904836; 31966601; 31966567; 32009276; 32069693; 32293623; 32358276; 32376414; 32386326; 32406271; 32555412; 32641144; 32668023; 32704409; 32680594; 32766304; 32848917; 32869039; 32920482; 32937655; 32957628; 32981508; 33111401; 33123220; 33123245; 33123250; 33200852
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
- The recall ran for 19 months, from 23 June 2023 to termination on 5 February 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 12 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: California, Delaware, Illinois, Louisiana, Michigan, Minnesota, Missouri, Ohio, Pennsylvania, Texas, Virginia, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Every product in this recall
The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2023-07-12 | Cargill Tripotassium Citrate Monohydrate packaged in 50 lb. paper bag. Product item: SKU 100105392, TPC GNLR 50LB BG KH FCC | Cargill, Inc Corporate Headquarters | Potential for foreign material (metal). | Class II |
Other records from Cargill, Inc Corporate Headquarters
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 29 other records name this firm.
All 30 records for Cargill, Inc Corporate Headquarters
All 2023 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.