Summary
The FDA issued a Class I for Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g) by LQNN Inc.. Reason: Undeclared allergen; egg.
Details
Source
Food Recall
External ID
F-1047-2024
Action Date
2024-03-13
Status
Terminated
Category
food
Product Description
Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
Lot/Code Info: Universal Product Code: 8 936014 313077 Lot #s: DEC0925, NOV2725, NOV1625, NOV1325, NOV0425, OCT1325, OCT0225
Quantity Affected: 222,320 bags (total)
Reason for Recall
Undeclared allergen; egg
Distribution
U.S. distribution to customers in: Alabama, Arizona, Arkansas, California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Tennessee, Texas, Utah, Virginia, and Washington. Canada with different product code and name: Banh Pia Hopia Cake Gateau Hopia
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-20
Company
Garden Grove, CA
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 124 food recalls issued in the same week, part of 204 food-related FDA actions this month.
LQNN Inc. has 12 FDA actions in our database, including 12 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 (LQNN Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LQNN Inc. have FDA actions?
LQNN Inc. has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1047-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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