PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported May 10, 2023

PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF MNCD 50LB BG/36P, paper bag

Products with a gluten free claim may contain gluten levels above 20 ppm.

Recall #
F-0786-2023
Affected scope
265,100 lbs
Initiated
March 30, 2023
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The recall

Cargill, Inc Corporate Headquarters issued this moderate-severity FDA Food recall — Products with a gluten free claim may contain gluten levels above 20 ppm..

Moderate
severity level
Class II
classification
May 10, 2023
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0786-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-0786-2023) was formally reported on May 10, 2023, with the manufacturer initiating the action on March 30, 2023. It is classified under Moderate severity (Class II), with a current status of Terminated. Cargill, Inc Corporate Headquarters is listed as the recalling firm, operating out of Wayzata, MN. Federal records list the affected scope as 265,100 lbs.

The documented reason for this recall is: Products with a gluten free claim may contain gluten levels above 20 ppm. Distribution data in the federal record shows the product reached: Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Food recalls over time

Where this recall sits in its category — 25,414 food recalls on record

-1,00001,0002,0003,000 20052008201120142017202020232026 436

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.

Severity

Moderate

Affected scope

265,100 lbs

Related Recalls

6

6 from same agency

Product description

PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF MNCD 50LB BG/36P, paper bag

Reason for recall

Products with a gluten free claim may contain gluten levels above 20 ppm.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-0786-2023
Date reported May 10, 2023
Date initiated March 30, 2023
Recalling firm Cargill, Inc Corporate Headquarters
Firm location Wayzata, MN
Affected scope 265,100 lbs
Distribution Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-0786-2023) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting — recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF MNCD 50LB BG/36P, paper bag. Recalled by Cargill, Inc Corporate Headquarters. Units affected: 265,100 lbs.
Why was this product recalled?
Products with a gluten free claim may contain gluten levels above 20 ppm.
Which agency issued this recall?
This recall was issued by the FDA Food on May 10, 2023. Severity: Moderate. Recall number: F-0786-2023.
Where was the recalled product distributed?
Distribution: Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-0786-2023) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Butter Parsley Bagel Crisps, Item Number 18490, Net Weight:… →

Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 10, 2023.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.