Food Recall Check
Class I · High risk Terminated Initiated May 14, 2024 (2 years ago)

S&S Cup Saimin-Noodles with Soup & Garnish recall

Recalled by H & U Inc. dba Sun Noodle · Honolulu, HI, United States

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

Why it was recalled

Undeclared egg

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

S&S Cup Saimin-Noodles with Soup & Garnish, NET WT. 5 oz., UPC 085315089056 and 085315089070

Quantity: 39,522 cases

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.

Year 2023: Lot codes 1623129 - 1623365 (May 9th, 2023 - December 31st, 2023) Year 2024: Lot codes 1624001 - 1624129 (January 1st, 2024 - May 8th, 2024)

Where it was sold

California Hawaii Nevada Utah

FDA's distribution note: U.S. distribution to the following: HI, CA, NV, UT No foreign distribution.

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
H & U Inc. dba Sun Noodle
Initiated by
Voluntary: Firm initiated
Recall initiated
May 14, 2024
In FDA report of
Jun 19, 2024
Terminated
Aug 8, 2024
FDA recall number
F-1346-2024 · event 94651
Official record
FDA enforcement report search

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