PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported February 26, 2020

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

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

Recall #
F-0769-2020
Affected scope
7660 bottles
Initiated
February 13, 2020
Verify with FDA Food →
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Suja Life LLC recalled Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234 — a moderate-severity action.

Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234 was recalled by Suja Life LLC in February 26, 2020. Reason: Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice …. Check the official notice for the remedy. Verify recall #F-0769-2020 with the FDA Food before acting.

The recall

Suja Life LLC issued this moderate-severity FDA Food recall — Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice ….

Moderate
severity level
Class II
classification
February 26, 2020
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0769-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-0769-2020) was formally reported on February 26, 2020, with the manufacturer initiating the action on February 13, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Suja Life LLC is listed as the recalling firm, operating out of Oceanside, CA. Federal records list the affected scope as 7660 bottles.

The documented reason for this recall is: Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Food recalls over time

Where this recall sits in its category — 25,414 food recalls on record

-1,00001,0002,0003,000 20052008201120142017202020232026 436

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

7660 bottles

Related Recalls

6

6 from same agency

Product description

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

Reason for recall

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

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-0769-2020
Date reported February 26, 2020
Date initiated February 13, 2020
Recalling firm Suja Life LLC
Firm location Oceanside, CA
Affected scope 7660 bottles
Distribution 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.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-0769-2020) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting — recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234. Recalled by Suja Life LLC. Units affected: 7660 bottles.
Why was this product recalled?
Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.
Which agency issued this recall?
This recall was issued by the FDA Food on February 26, 2020. Severity: Moderate. Recall number: F-0769-2020.
Where was the recalled product distributed?
Distribution: 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 do I check if my product is affected by a recall?
Check the product description and recall number (F-0769-2020) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported February 26, 2020.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.