FDA recall record

DANONE Silk Soymilk Vanilla Bag-In-Box recall — FDA F-2244-2019

Mislabeled outer box of Silk Soymilk Vanilla Bag-In-Box. Outer box incorrectly indicates the product is almond milk instead of soymilk. The internal…

Class IIclassification
F-2244-2019official record ID
Oct 2, 2019report date

Recall record at a glance

Official recordF-2244-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDANONE
Report dateOct 2, 2019
Recall initiation dateSep 5, 2019
Quantity46 Cases
LocationMount Crawford, VA, United States

Official product description

Silk Soymilk Vanilla Bag-In-Box. One, 2.5 gallon bag per box. 2.5 gal Bag-In-Box to be used in a dispensing machine at foodservice & convenience outlets.

Why the product was recalled

Mislabeled outer box of Silk Soymilk Vanilla Bag-In-Box. Outer box incorrectly indicates the product is almond milk instead of soymilk. The internal product in box is labeled correctly as Silk Soymilk Vanilla Bag-In-Box.

Distribution information

The product was shipped to 3 locations of Dot Foods, Inc. 3 States: Arizona, California, Indiana.

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.