Recall record at a glance
| Official record | F-0788-2021 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Heidi Remington |
| Report date | Jul 28, 2021 |
| Recall initiation date | Jun 18, 2021 |
| Quantity | 72 units |
| Location | Talent, OR, United States |
Official product description
Heidi's Brownies is packaged in saran wrap in a plastic bag with a twist tie, 3 oz (85g). Label is read in parts: "***Heidi's ~~~ Brownies ~~~ *Malted barley wheat flour, cane sugar, water, chocolate chips (unsweetened chocolate, sugar, dextrose, soy lecithin (an emulsifier)(may contain milk), Non-GMO Canola oil, cocoa, apple cider vinegar, vanilla ***almond ext (May Contains Nuts), sodium bicarbonate, cinnamon, sea salt, demerara sugar ***Contains: Wheat, almonds *** Heidis Pie in the Sky Talent, OR 97540 ***".
Why the product was recalled
Soy Lecithin listed in ingredients statement but soy is not mentioned in the contains statement.
Distribution information
distributed in OR only.
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: Telephone.
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.