Recall record at a glance
| Official record | F-0182-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | fayeon distributors Inc. |
| Report date | Dec 7, 2022 |
| Recall initiation date | Oct 21, 2022 |
| Quantity | 194 cases. 12 units per case |
| Location | Montclair, CA, United States |
Official product description
Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung bean powder (cereal containing gluten), sugar, almond (tree nuts), vegetable oil (canola oil), peanuts; (may contain traces of walnut, egg, and milk). Packed in cases of 12 units Store in cool, dry place 400g (14 oz.) UPC Code: 6 50495 00056 8 Made in Macau
Why the product was recalled
Product may contain undeclared milk
Distribution information
A total of 20 customers received this product located in NY and CA
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.