Givaudan Nat Chicken Flavor Recall: Salmonella Risk in 18.144kg Packages
Givaudan recalls 18.144kg Nat Chicken rotisserie flavor packages with Salmonella contamination. Consumers should check for brown square boxes with blue plastic interior and batch number DV00295989.
Recall notice
Positive Salmonella sp. in product
Contact the company
What happened, in plain English
Givaudan is recalling 18.144kg packages of Nat Chicken rotisserie flavor due to Salmonella contamination. This poses a health risk if the product is consumed, as Salmonella can cause food poisoning. Read more at govinfonow.com/recall/13991-givaudan-nat-chicken-flavor-recall-salmonella-risk-in-18-144kg.
Source Summary by GovInfoNow · govinfonow.com/recall/13991-givaudan-nat-chicken-flavor-recall-salmonella-risk-in-18-144kg · Updated October 4, 2026 · FDA enforcement record: FDA #F-0094-2022
Cite this page
“Givaudan Nat Chicken Flavor Recall: Salmonella Risk in 18.144kg Packages.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13991-givaudan-nat-chicken-flavor-recall-salmonella-risk-in-18-144kg. Based on FDA recall #F-0094-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0094-2022%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. The product was found to contain positive Salmonella sp. which means it is contaminated with harmful bacteria.
Who’s affected
Anyone who purchased the 18.144kg Nat Chicken rotisserie flavor packages with brown square boxes and blue plastic interiors. People who use these products for cooking or food preparation are most at risk.
How to tell if you have this one
Check for packages labeled 'AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg' in brown square boxes with blue plastic interiors. The batch number is DV00295989 and expiration date is 10/13/22.
- Brand
Givaudan- Category
Food
What to do — step by step
Check Product Details
Look for brown square boxes with blue plastic interiors and batch number DV00295989 on the package.
Where it went and when
Where it was distributed
Distributed in Indiana.
FDA distribution: “100% of product was shipped to single account in Indiana” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-0094-2022 (October 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0094-2022 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.