Recall record at a glance
| Official record | F-2083-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Sunshine Bakery |
| Report date | Apr 26, 2017 |
| Recall initiation date | Mar 24, 2017 |
| Quantity | 320 units |
| Location | Alhambra, CA, United States |
Official product description
Cassava Cake (Khoa Mi) in strips or cake form, individually packaged in clear wrap and Styrofoam tray, with a printed label on top. Best by date is printed on the label. 5 oz/141 grams per unit with UPC code 015200401304
Why the product was recalled
The products are being recalled because the labeling does not declare food allergens peanuts, coconuts, almonds and cashews on the label..
Distribution information
Products were distributed to retail stores in California, Texas and Nevada.
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: Press Release.
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.