FDA recall record

Suja Life 12 oz recall — FDA F-0769-2020

Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.

Class IIclassification
F-0769-2020official record ID
Feb 26, 2020report date

Recall record at a glance

Official recordF-0769-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSuja Life LLC
Report dateFeb 26, 2020
Recall initiation dateFeb 13, 2020
Quantity7660 bottles
LocationOceanside, CA, United States

Official product description

Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234

Why the product was recalled

Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.

Distribution information

One consignee with distribution centers in CA, NJ, GA, FL, NC, TX, IN, OH, MA, WI, CO, MI, VI, MN, PA, IA, NH, MD, IL, NY, MA and retail locations throughout the United States.

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: Letter.

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.

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Suja Life 12 oz recall — FDA F-0770-2020

Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.

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Suja Life 12 oz recall — FDA F-0772-2020

Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.

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Suja Life 12 oz recall — FDA F-0771-2020

Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.

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