Givaudan Natural Mirepoix Flavor Recall: Metal Fragments Found
Givaudan recalls Natural Mirepoix Flavor 181.4 kg drums due to metal fragments. Consumers should check lot numbers DV00187909, DV001900068, DV00192593 for affected products.
Lower-risk recall
The firm was notified of metal fragments in the product.
Contact the company
What happened, in plain English
Givaudan is recalling Natural Mirepoix Flavor 181.4 kg drums because metal fragments were found in the product. This could pose a risk of injury if the metal pieces are ingested. Read more at govinfonow.com/recall/20099-givaudan-natural-mirepoix-flavor-recall-metal-fragments-found.
Source Summary by GovInfoNow · govinfonow.com/recall/20099-givaudan-natural-mirepoix-flavor-recall-metal-fragments-found · Updated October 7, 2026 · FDA enforcement record: FDA #F-0374-2018
Cite this page
“Givaudan Natural Mirepoix Flavor Recall: Metal Fragments Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20099-givaudan-natural-mirepoix-flavor-recall-metal-fragments-found. Based on FDA recall #F-0374-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0374-2018%22&limit=1).
Why it’s dangerous
Metal fragments can be ingested accidentally when the flavor is used in food preparation. This poses a risk of injury if the metal pieces are swallowed.
Who’s affected
Anyone who purchased the Natural Mirepoix Flavor 181.4 kg drums with lot numbers DV00187909, DV001900068, or DV00192593. Food manufacturers using this flavor in products are most at risk.
How to tell if you have this one
Check the lot numbers on the drum: DV00187909, DV001900068, or DV00192593. The product is a 181.4 kg drum of Natural Mirepoix Flavor containing carrot juice, celery juice concentrate, and other ingredients.
- Brand
Givaud: Natural Flavors- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers DV00187909, DV001900068, or DV00192593 on the drum.
Where it went and when
Where it was distributed
Distributed in Wisconsin.
FDA distribution: “Product was shipped to WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Wisconsin.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0374-2018 (November 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0374-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.