RecallHawk
Class I Recall

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

HAR Maspeth Corp.

Summary

The FDA issued a Class I for Jinga Glass Noodles with vegetables 8 oz. and 12 oz. by HAR Maspeth Corp.. Reason: Contains undeclared egg.

Details

Source

Food Recall

External ID

F-0663-2025

Action Date

2025-04-02

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 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

Quantity Affected: 2,627 packages

Reason for Recall

Contains undeclared egg

Distribution

NY, NJ, MA, CT, PA, MD, NC, IL, MI, GA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-14

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (HAR Maspeth Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does HAR Maspeth Corp. have FDA actions?

This is the only FDA action we have on record for HAR Maspeth Corp. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0663-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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