Food Recall Check
Class I · High risk Terminated Initiated Oct 3, 2025 (12 months ago)

Twin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE recall

Recalled by Twin Marquis, LLC · Brooklyn, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product contains undeclared egg, FD&C Yellow 5, and FD&C Yellow 6.

Undeclared allergen: Egg

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Twin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE; NET WT 16 OZ; Ingredients: Bleached Wheat Flour, Water, Corn Starch, Salt, Sodium Benzoate (For Freshness); Contains: Wheat.; Produced on machinery that uses eggs; Manufactured by: Twin Marquis Inc. Brooklyn, NY 11206; UPC 7 60941 10301 6

Quantity: 5080 packages

Food: Pasta, rice & grains

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.

Date code "05520" stamped on the back of the package

Where it was sold

Connecticut Florida Illinois Maryland New Jersey New York

FDA's distribution note: IL, MD, NJ, NY, FL, CT

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Twin Marquis, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 3, 2025
In FDA report of
Oct 29, 2025
Terminated
Feb 11, 2026
FDA recall number
H-0184-2026 · event 97752
Official record
FDA enforcement report search

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