LQNN Inc. recalls BANH PIA Hopia Cake Mungbean Durian (9.7oz) due to undeclared egg allergen. Consumers should check lot numbers NOV1625 and OCT1525 for affected products.
Undeclared allergen; egg
LQNN Inc. is recalling BANH PIA Hopia Cake Mungbean Durian products because they contain undeclared egg, which poses a risk for people with egg allergies. This recall affects specific lot numbers sold in November and October 2015.
The product contains egg without being declared as an allergen. This can cause allergic reactions in individuals sensitive to egg, particularly those with severe allergies who may experience symptoms like hives, swelling, or difficulty breathing.
People with egg allergies may be affected by this recall. Those who purchased the product with lot numbers NOV1625 or OCT1:25 are most at risk.
Check the product label for the brand name LQNN Inc. and product name BANH PIA Hopia Cake Mungbean Durian. Look for lot numbers NOV1625 or OCT1525 on the packaging.
Look for lot numbers NOV1625 or OCT1525 on the packaging to identify affected products.
No, this product contains undeclared egg, which can cause allergic reactions in people with egg allergies.
Check the product label for lot numbers NOV1625 or OCT1525. If you have these lot numbers, stop using the product and contact LQNN Inc. for further instructions.
The product must be labeled as BANH PIA Hopia Cake Mungbean Durian with lot numbers NOV1625 or OCT1525.
We’ve drafted a message you can send LQNN Inc. to request your refund or repair — edit it as you like.
Subject: Recall F-1048-2024 — LQNN Inc. LQNN Inc. Hello, I own a LQNN Inc. that is covered by recall F-1048-2024 from LQNN Inc.. 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.
