FDA recall record

Dolcetta Artisan Sweets Peppermint Caramel Truffles are dark chocolate truffle with recall — FDA F-1942-2017

undeclared soy lecithin and milk (cream was declared).

Class IIclassification
F-1942-2017official record ID
Apr 19, 2017report date

Recall record at a glance

Official recordF-1942-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDolcetta Artisan Sweets
Report dateApr 19, 2017
Recall initiation dateMar 6, 2017
Quantity100 boxes
LocationSeattle, WA, United States

Official product description

Peppermint Caramel Truffles are dark chocolate truffle with peppermint and caramel, 3.9 oz (110g), individually wrapped in clear cellophane and then wrapped in a paper box. The label declared "***Peppermint Caramel Truffles***60% dark chocolate, 72% dark chocolate, cane sugar, cream, cocoa powder, peppermint extract, salt, vanilla bean***".

Why the product was recalled

undeclared soy lecithin and milk (cream was declared).

Distribution information

distributed in OR and WA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.