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Ardent Mills, LLC

Complete recall history across all FDA and CPSC categories — 8 total recalls

Ardent Mills, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (8)

FDA food safety enforcement actions by Ardent Mills, LLC

Date Product Reason Class
May 18, 2022 BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine... Potential to contain small pieces of stainless steel from a piece of milling ... Class II
Feb 10, 2022 Ardent Mills Hotel and Restaurant All Purpose Flour - AA, 50 lb. (22.68kg) ba... Raw, untreated flour tested positive for Salmonella. Class II
Jan 4, 2019 ARDENT H&R SR FLR, 25LB, 50 LB, and 25LB (PC)-309951, packaged in paper bags,... Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour becau... Class II
Jan 4, 2019 HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour becau... Class II
Jan 4, 2019 WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour becau... Class II
Jan 4, 2019 MEMBERS MARK SELF RISE FLR 25LB Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour becau... Class II
Sep 13, 2018 Safeguard Soft Flr (GIV) packaged in 50 lb bags Flour tested positive for Salmonella by customer. Class II
Jun 2, 2017 PRIMO MOLINO ITALIAN STYLE ENRICHED FLOUR, 50 lb, Packaged in paper bags, Sto... Primo Molino Italian Style Flour may be contaminated with E. coli O121. Class I

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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