LQNN Inc. Recall: Undeclared allergen; egg

🇺🇸 United States

1. February 20, 2024 - Recall initiated
2. March 13, 2024 - Reported by source
3. May 14, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1042-2024

Event ID

94085

Status

Terminated

Classification

Class I

Company

LQNN Inc.

Product description

BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)

Quantity

222,320 bags (total)

Reason

Undeclared allergen; egg

Recall initiation date

February 20, 2024

Report date

March 13, 2024

Classification date

Not published in this source record

Termination date

May 14, 2024

Distribution pattern

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

UPC, lot, and code information

Universal Product Code: 8 936014 318942. Lot #s: B4.12.23; B6.12.23; B1.11.23; B2.11.23; B3.11.23; A7.11.23; A8.11.23; A9.11.23; A1.11.23; A2.11.23; A3.11.23; A4.11.23; C9.10.23; C10.10.23; C11.10.23; C6.10.23; C7.10.23; C8.10.23; C2.10.23; C3.10.23; C4.10.23; C5.10.23; C1.10.23; B10.10.23; B4.10.23; B5.10.23; B6.10.23; B7.10.23; B8.10.23; B1.10.23; B2.10.23; A10.10.23

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 94085 with 10 other product entries in Public Health Trace.

Responsible company: LQNN Inc.

Other recalls from LQNN Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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