FDA recalls Banh Pia Classic Hopia for undeclared egg allergen
LQNN Inc. is recalling Banh Pia Classic Hopia because it contains undeclared egg allergen, which can cause serious allergic reactions. About 222,320 bags were distributed across 31 U.S. states and Canada.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I recall as classified by the agency. The rule specifies FDA Class I recalls never score below 4. Undeclared egg allergen poses a documented health risk to allergic consumers, though no illnesses have been reported in the source.
Plain-English summary
LQNN Inc. is recalling Banh Pia Classic Hopia, Mung Bean Durian flavor (16.8oz/480g bags), because the product contains undeclared egg allergen. This poses a serious health risk to consumers with egg allergies.
The recall affects 222,320 bags distributed to customers across 31 U.S. states and Canada. In Canada, the product was sold under the name Banh Pia Hopia Cake Gateau Hopia with a different product code.
Consumers who purchased this product should stop consumption immediately if they have an egg allergy. The affected product has Universal Product Code 8 936014 313077. Affected lot numbers are: DEC0925, NOV2725, NOV1625, NOV1325, NOV0425, OCT1325, and OCT0225.
The recalled product
- Product
- Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
- Manufacturer
- LQNN Inc.
- Category
- Food — Baked Goods
- Hazard
- Affected units
- 222,320
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- Universal Product Code: 8 936014 313077 Lot #s: DEC0925
- NOV2725
- NOV1625
- NOV1325
- NOV0425
- OCT1325
- OCT0225
Distribution
Part of a larger recall action
This product is one of 12 recalled by LQNN Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 12 products in this recall →Related recalls
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