Food Recall Check
Class I · High risk Terminated Initiated Mar 14, 2025 (2 years ago)

Jinga Glass Noodles with vegetables recall

Recalled by HAR Maspeth Corp. · Maspeth, NY, United States

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

Why it was recalled

Contains 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

Jinga Glass Noodles with vegetables 8 oz. and 12 oz.

Quantity: 2,627 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.

Expiration date(s) or Use by Date(s) or expected shelf life of product: 3/13/2025, 3/1/2025, 3/15/2025, 3/16/2025, 3/17/2025, 3/18/2025. UPC Codes: 265405006495, 267405004495, 266405008496, 268405005499 Catalog numbers: 5405, 7405, 6405M, 8405M

Where it was sold

Connecticut Georgia Illinois Massachusetts Maryland Michigan North Carolina New Jersey New York Pennsylvania

FDA's distribution note: NY, NJ, MA, CT, PA, MD, NC, IL, MI, GA

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
HAR Maspeth Corp.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 14, 2025
In FDA report of
Apr 2, 2025
Terminated
Mar 5, 2026
FDA recall number
F-0663-2025 · event 96503
Official record
FDA enforcement report search

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