VEGETARIAN CHICKEN FLAVOR RAMEN Express
Reason Product contains undeclared Yellow #5
VEGETARIAN CHICKEN FLAVOR RAMEN Express recall
Recalled by Palmetto Gourmet Foods Inc. · Saluda, SC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared Yellow #5
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Vegetable oil***" Contains: Wheat, Soy. UPC 8 10037 81061 5 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
Quantity: 5,664,960/3oz pkgs
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
All products with Best By Date before 01/15/2027
Where it was sold
Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Michigan Missouri Mississippi North Carolina Nebraska New Hampshire New Jersey New York Ohio Oklahoma Oregon Pennsylvania Tennessee Texas Utah Virginia Wisconsin
FDA's distribution note: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA & WI.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.
- Recalling firm
- Palmetto Gourmet Foods Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 17, 2026
- In FDA report of
- Mar 18, 2026
- FDA recall number
- H-0547-2026 · event 98313
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.