The Recall Desk
SevereFDA (Food)·F-1947-2017·Announced 2017-04-19

Dolcetta S'more Bars Recalled for Undeclared Soy and Milk Allergens

Dolcetta Artisan Sweets is recalling 50 S'more Bars in Oregon and Washington due to undeclared soy lecithin and milk.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 per the rubric, despite the hazard being undeclared allergens.

Plain-English summary

Dolcetta Artisan Sweets is recalling 50 units of S'more Bars, 1.2 oz (33g), because the product contains undeclared soy lecithin and milk. The product consists of dark chocolate and toasted white chocolate with graham cracker, wrapped in metal foil and a paper box. The label declared ingredients including 60% dark chocolate, 32% white chocolate, graham crackers (wheat), and vanilla bean, but did not list the soy and milk allergens.

The affected products were distributed in Oregon and Washington. The recall was initiated by the U.S. Food and Drug Administration under recall number F-1947-2017.

Consumers with allergies to soy or milk should avoid consuming the product. The source text does not specify further consumer instructions or report any illnesses.

The recalled product

Product
S'more Bar contains dark chocolate and toasted white chocolate with graham cracker, 1.2 oz (33g), Product wrapped in metal foil and then wrapped in paper box. The label declared "***SMores Bar *** 60% dark chocolate, 32% white chocolate, graham crackers (wheat), vanilla bean *
Affected units
50

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • none

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 26 recalled by Dolcetta Artisan Sweets under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 26 products in this recall →