PROSANTE TVGPTN 12BF7 MNCD 50LB BG/36P, paper bag
Cargill, Inc Corporate Headquarters recalled this product and the FDA reported the enforcement action on 10 May 2023 as Class II. The recall was initiated by the firm. Products with a gluten free claim may contain gluten levels above 20 ppm.
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
- PROSANTE TVGPTN 12BF7 MNCD 50LB BG/36P, paper bag
- Reason for recall
- Products with a gluten free claim may contain gluten levels above 20 ppm.
- Recalling firm
- Cargill, Inc Corporate Headquarters
- Firm location
- Wayzata, Minnesota, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0792-2023
- Quantity
- 39,600 lbs
- Distribution
- Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
- Initiated
- 30 March 2023
- Reported by FDA
- 10 May 2023
- Terminated
- 8 June 2023
- Firm notified by
- Product codes
- 100001377-36022CHXEA
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 22 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 22 separate recalls, which almost every published figure does, overstates it by a factor of 22. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 22 of them.
- The recall ran for 2 months, from 30 March 2023 to termination on 8 June 2023. 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 FDA published the enforcement report 6 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.
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
Behind every recall is a clause 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.