FDA recall record

Double-Cola Co.-USA dba The Double Cola Company Cherry SKI LEMON ORANGE AUTHENTIC CITRUS recall — FDA F-0908-2018

The firm was notified by a customer that the product label did not list the allergens Yellow #5 & Red 40.

Class IIclassification
F-0908-2018official record ID
Mar 14, 2018report date

Recall record at a glance

Official recordF-0908-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDouble-Cola Co.-USA dba The Double Cola Company
Report dateMar 14, 2018
Recall initiation dateFeb 16, 2018
Quantity200cs/12/12oz cans
LocationChattanooga, TN, United States

Official product description

Cherry SKI LEMON ORANGE AUTHENTIC CITRUS SODA 12 oz can CONTAINS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, LEMON JUICE CONCENTRATE, ORANGE JUICE CONCENTRATE, CITRIC ACID, NATURAL FLAVOR, SODIUM BENZOATE (PRESERVATIVE), CAFFEINE, CELLULOSE GUM, RED #4, GUM ARABIC, BLUE #1. UPC: 0 71644 20103 0

Why the product was recalled

The firm was notified by a customer that the product label did not list the allergens Yellow #5 & Red 40.

Distribution information

Products were distributed in IL, IN, KY and OH.

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.