RecallHawk
Class I Recall

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

H & U Inc. dba Sun Noodle

Summary

The FDA issued a Class I for S&S Cup Saimin-Noodles with Soup & Garnish, NET WT. 5 oz., UPC 085315089056 and by H & U Inc. dba Sun Noodle. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

F-1346-2024

Action Date

2024-06-19

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 39,522 cases

Reason for Recall

Undeclared egg

Distribution

U.S. distribution to the following: HI, CA, NV, UT No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-14

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 88 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 (H & U Inc. dba Sun Noodle) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does H & U Inc. dba Sun Noodle have FDA actions?

This is the only FDA action we have on record for H & U Inc. dba Sun Noodle in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1346-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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