Recall archive / FDA food enforcement
BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g) — FDA record F-1042-2024
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 20, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)
- Reason
- Undeclared allergen; egg
- Classification
- Class I
- Recalling firm
- LQNN Inc.
- Quantity
- 222,320 bags (total)
- Agency-reported status
- Terminated
- Source record identifier
- F-1042-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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 |
Match all identifying details in the current notice. A brand name alone is not enough.
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
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Mar 13, 2024
- Recall initiation date
- Feb 20, 2024
- Center classification date
- Mar 7, 2024
- Termination date
- May 14, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.