RecallHawk
Class I Recall

Large 4- Date Mooncake Gift Box

Sheng Kee of California, Inc dba Sheng Kee Bakery

Summary

The FDA issued a Class I for Large 4- Date Mooncake Gift Box by Sheng Kee of California, Inc dba Sheng Kee Bakery. Reason: Undeclared allergen; egg..

Details

Source

Food Recall

External ID

F-0289-2024

Action Date

2023-10-25

Status

Terminated

Category

food

Product Description

Large 4- Date Mooncake Gift Box

Lot/Code Info: All dates within expiry.

Quantity Affected: N/A

Reason for Recall

Undeclared allergen; egg.

Distribution

U.S. distribution to the following: CA, IL, TX, GA, WA, and NJ No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-09-01

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 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Sheng Kee of California, Inc dba Sheng Kee Bakery has 5 FDA actions in our database, including 5 recalls.

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 (Sheng Kee of California, Inc dba Sheng Kee Bakery) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sheng Kee of California, Inc dba Sheng Kee Bakery have FDA actions?

Sheng Kee of California, Inc dba Sheng Kee Bakery has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0289-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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