FDA recall record

Yukon Jackson Herd of Turtles confection dark chocolate, 4 oz recall — FDA F-1577-2018

Herd of Turtles confection dark chocolate is recalled because pecan is listed on the Ingredients statement but it is not listed in the Contains statement.

Class IIIclassification
F-1577-2018official record ID
Jun 20, 2018report date

Recall record at a glance

Official recordF-1577-2018
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmYukon Jackson
Report dateJun 20, 2018
Recall initiation dateMay 25, 2018
Quantity6 cs + 2 lbs. bulk of 8 oz and 160 unit of 4 oz
LocationSeattle, WA, United States

Official product description

Herd of Turtles confection dark chocolate, 4 oz. and 8 oz. packages. UPC of 4 oz: 6 55974 89005 0. UPC of 8 oz: 6 55974 89007 4. The label is read in parts: "***INGREDIENTS: BITTERSWEET CHOCOLATE 60% (COCOA LIQUOR, SUGAR, EMULSIFIER, SOYA LECITHIN, VANILLA) ***CARAMEL (SUGAR, CREAM, MILK, CORN SYRUP, COCOA BUTTER), ***PECANS***CONTAINS: MILK & SOYA ***".

Why the product was recalled

Herd of Turtles confection dark chocolate is recalled because pecan is listed on the Ingredients statement but it is not listed in the Contains statement.

Distribution information

distributed in WA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: 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.