Food recall
Moonstruck Chocolate Company recall: The Salty Nutty Toffee Bar, brand ALMA
Moonstruck Chocolate Company, of Portland, OR, recalled The Salty Nutty Toffee Bar, brand ALMA. The FDA's reason: “the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on December 7, 2018, and the FDA first listed it in its Enforcement Report of December 26, 2018. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class II
It could cause temporary or minor harm
Why
Allergen not on the label
Status
Terminated
Closed February 25, 2019
The recall
- Company
- Moonstruck Chocolate Company (Portland, OR)
- Reason, in FDA's words
- “the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin”
- Where it was sold
- Distributed in CA, MD, NC, ND, NY, OR and UT.
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 81744
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0750-2019 Class II
The Salty Nutty Toffee Bar, brand ALMA, net weight 1.85 oz. UPC on individual bar: 8 58533 00602 8 UPC on master case 0 108585 330060 2 The label is read in parts: "***INGREDIENTS: Salty Nutty Toffee Bar *** Dark Chocolate (cocoa solids, cocoa butter, sugar, sunflower lecithin), Toffee (turbinado sugar, butter (milk, salt), Pistachios, Hazelnuts, Sea Salt. Contains: Milk, Nuts***ALMA HANDMADE CHOCOLATES 140 Northeast 28th Avenue Portland, OR 97232***".
Codes: MAR 30, 2019
Quantity: 323 bars
Get new charts weekly
One email a week with the newest charts and their key numbers. No account needed.
Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of December 26, 2018.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.