Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)

LQNN Inc. recalled this product and the FDA reported the enforcement action on 13 March 2024 as Class I. The recall was initiated by the firm. Undeclared allergen; egg

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product

Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)

Reason for recall

Undeclared allergen; egg

Recalling firm

LQNN Inc.

Firm location

Garden Grove, California, United States

Classification

Class I

Status

Terminated

Recall number

F-1047-2024

Quantity

222,320 bags (total)

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

Initiated

20 February 2024

Reported by FDA

13 March 2024

Terminated

14 May 2024

Firm notified by

Letter

Product codes

Universal Product Code: 8 936014 313077 Lot #s: DEC0925, NOV2725, NOV1625, NOV1325, NOV0425, OCT1325, OCT0225

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

• Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
• The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
• This is one of 12 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 12 separate recalls, which almost every published figure does, overstates it by a factor of 12. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 12 of them.
• The recall ran for 3 months, from 20 February 2024 to termination on 14 May 2024. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
• The FDA published the enforcement report 3 weeks after the firm began the recall.
• The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

What this recall was for

The allergens named in this record: eggs.

Other records from LQNN Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 11 other records name this firm.

All 12 records for LQNN Inc.

All 2024 recalls · All FDA food recall data