Recall record at a glance
| Official record | F-1654-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Nectar Foods LLC |
| Report date | Jul 18, 2018 |
| Recall initiation date | Jun 21, 2018 |
| Quantity | 79 display cases or sleeves (948 bars total) |
| Location | Portland, OR, United States |
Official product description
Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker label. Net wt. 2.5 oz, 3" x 3" bar, 12 bars to a cardboard display case and 12 display cases to a cardboard master case. UPC on each bar is 8 54835 00402 9. The product label is read in parts: "***Paleo HONEY MAMA'S***Oregon Peppermint CACAO-NECTAR BAR ***Made with luscious coconut meat, dark cocoa, peppermint oil & raw local honey*** NO Gluten, Soy, Dairy or Grain *** INGREDIENTS: raw local honey, shredded Organic coconut, unrefined Organic coconut oil, Organic Dutch alkalized cocoa powder, Himalayan pink salt, peppermint oil***Contains tree nut (coconut).
Why the product was recalled
Honey Mama's Oregon Peppermint Cacao-Nectar Bar, 2.5 oz, is recalled due to undeclared almonds.
Distribution information
Product is sold on website HoneyMamas.com and distributed in Arkansas, California, Delaware, Florida, Georgia, Louisiana, Massachusetts, New Jersey, New York, North Carolina, Ohio, Oregon, Texas, Utah, Virginia, Vermont, Washington and Wisconsin.
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: 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.
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