FDA recall record

TN Juice Bar Refine 3-Day Cleanse, a juice kit that contains Lean Green, 16 recall — FDA F-0265-2016

Unpasteurized juice product with elevated pH levels and unlabeled almond milk were distributed.

Class Iclassification
F-0265-2016official record ID
Dec 2, 2015report date

Recall record at a glance

Official recordF-0265-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTN Juice Bar
Report dateDec 2, 2015
Recall initiation dateSep 4, 2015
Quantity137 units
LocationHendersonville, TN, United States

Official product description

Refine 3-Day Cleanse, a juice kit that contains Lean Green, 16 oz (6 bottles), Beet It, 16 oz (6 bottles), Almond Milk, 8 oz (3 bottles) and Wheat grass juice, 8 oz (2 bottles)

Why the product was recalled

Unpasteurized juice product with elevated pH levels and unlabeled almond milk were distributed.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.