Recall record at a glance
| Official record | F-0350-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Heidi Remington |
| Report date | Feb 22, 2023 |
| Recall initiation date | Jan 12, 2023 |
| Quantity | 76 packages |
| Location | Talent, OR, United States |
Official product description
Lemon Almond Blueberry Bread, UPC 7 21762 76434 3, Net wt.3.5oz (98g). The sliced Lemon Blueberry Bread is wrapped in a clear plastic shrink wrap. The label stated "***Lemon Almond Blueberry Bread* Malted barley wheat flour, milk, eggs, almonds...Contains: Wheat, eggs, milk, almonds***Heidi s Pie in the Sky, Talent, OR 97540***".
Why the product was recalled
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin
Distribution information
distributed in Oregon.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.