FDA recall record

Jus Made Roo's Juice Tropical Orange Flavor recall — FDA F-1539-2013

The product has the potential to contain polysaccharide-based bacterial biofilm, mold, and red water mites.

Class IIclassification
F-1539-2013official record ID
Jun 26, 2013report date

Recall record at a glance

Official recordF-1539-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmJus Made, Inc.
Report dateJun 26, 2013
Recall initiation dateMay 21, 2013
Quantity1,995 cases
LocationDallas, TX, United States

Official product description

Roo's Juice Tropical Orange Flavor (5% juice beverage) 10 FL OZ. (296 mL) Distributed by The Pantry, Inc. Sanford, NC 27330

Why the product was recalled

The product has the potential to contain polysaccharide-based bacterial biofilm, mold, and red water mites.

Distribution information

TX, NC, AR, AL, KY, MO, and GA

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.