Class IITerminated in FDA datasetRecall initiated Aug 12, 2015

Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt, sold under brand Willit House. Each bar…

Recalling firm: Willit House Chocolate Co

Why it was recalled

Undeclared soy lecithin. Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt contains soy lecithin but label does not declare soy.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 8, 2016.

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Compare the exact product and package details with the label you have.

ProductDark Chocolate with Cranberry, Roasted Nuts & Sea Salt, sold under brand Willit House. Each bar is wrapped in gold foil and then wrapped with a box. Each box contains 12 bars and each bar has a net weight 60 gram.
Package size60 gram

FDA code information

codes: C2215F, C2915F, D0215F, D0315F, D2815F, D3115F, E0415F. All have best by date of 05/31/16. The code C2215F breakdown as: The first letter is the month of manufacturing (A=April, B=May, C=June, etc). The first and second number are the dates of manufacture. The third and fourth number are the year of manufacture. The last letter is the location of manufacture.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt, sold under brand Willit House. Each bar is wrapped in gold foil and then wrapped with a box. Each box contains 12 bars and each bar has a net weight 60 gram.

Original FDA recall reason

Undeclared soy lecithin. Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt contains soy lecithin but label does not declare soy.

Recall details

Recall number
F-3066-2015
Event ID
71954
FDA status
Terminated
Initiated
Aug 12, 2015
Reported
Sep 9, 2015
Classified
Sep 1, 2015
Terminated
Apr 8, 2016
Quantity
318 bars
Location
North Pole, AK, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

distributed in Alaska only.

FDA source record · F-3066-2015

Data updated September 16, 2026. View official FDA data ↗

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