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