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Moonstruck Chocolate Company Recall: the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin

United States

TerminatedClass II

Company
Moonstruck Chocolate Company
Product
The Salty Nutty Toffee Bar, brand ALMA, net weight 1.85 oz.…
Recall date
December 7, 2018
Terminated
February 25, 2019
Source
FDA

Reason for recall

the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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***". Not published in this source record 323 bars MAR 30, 2019

Distribution

  • Distributed in CA
  • MD
  • NC
  • ND
  • NY
  • OR and UT.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0750-2019
Event ID
81744
Status
Terminated
Classification
Class II
Company
Moonstruck Chocolate Company
Product description
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***".
Quantity
323 bars
Reason
the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin
Recall initiation date
December 7, 2018
Report date
December 26, 2018
Classification date
Not published in this source record
Termination date
February 25, 2019
Distribution pattern
Distributed in CA, MD, NC, ND, NY, OR and UT.
UPC, lot, and code information
MAR 30, 2019
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Moonstruck Chocolate Company

Other recalls from Moonstruck Chocolate Company

FDA Recall United States Terminated Historical recordClass I

Moonstruck Chocolate Company

Product
Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocol…
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Moonstruck Chocolate Company

Product
Sea Salt Caramels Tumbled In Milk Chocolate, Moonstruck bran…
Published
January 2, 2019
Distribution
distributed in AZ, CA, ID, NH, NY, OR, T…

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Maryland 1
North Carolina 1
North Dakota 1
New York 1
Oregon 1
Utah 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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