LQNN recalls 16.8oz Banh Pia Classic Hopia Mung Bean Durian due to undeclared egg allergen. Affected lots from DEC0925 to OCT0225. Consumers should check product labels for egg presence.
Undeclared allergen; egg
LQNN is recalling Banh Pia Classic Hop: Mung Bean Durian products because they contain undeclared egg, which can cause allergic reactions in sensitive individuals. This recall affects specific production lots sold between late 2024 and early 2025.
The product contains egg as an allergen that was not declared on the label. This can cause allergic reactions in individuals sensitive to egg, potentially leading to symptoms like hives, swelling, or more severe reactions in rare cases.
People with egg allergies who consume these products may experience allergic reactions. The recall applies to specific lots produced from November 2024 through December 2024.
Check for the Universal Product Code (UPC) 8 936014 313077 on the product label. The affected lots include DEC0925, NOV2725, NOV1625, NOV1325, NOV0425, OCT1325, and OCT0225.
Look for the Universal Product Code (UPC) 8 936014 313077 on the product label to identify affected lots.
The recall record states the product contains undeclared egg, but does not explain why it was not declared.
Check for the Universal Product Code (UPC) 8 936014 313077 and the lot numbers DEC0925, NOV2725, NOV1625, NOV1325, NOV0425, OCT1325, or OCT0225.
The recall record does not specify a remedy, so consumers should check the product label for the UPC and lot numbers to determine if it is affected.
We’ve drafted a message you can send LQNN to request your refund or repair — edit it as you like.
Subject: Recall F-1047-2024 — LQNN LQNN Hello, I own a LQNN that is covered by recall F-1047-2024 from LQNN. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
