CLASS II Food recall · Reported 5 Jun 2019 · FDA Enforcement Report

Suja Organic Kombucha - Mixed Berries recalled by Suja Life

Suja Life is recalling Suja Organic Kombucha - Mixed Berries, distributed in 19 states. The recall was initiated on 20 May 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest by 7/29/19
Quantity recalled66,964 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1431-2019
FDA event ID
82898
Recalling firm
Suja Life, San Diego, CA
Brand
Suja
Classification
Class II
Status
Terminated
Recall initiated
20 May 2019
FDA classified
30 May 2019
Reported
5 Jun 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Tea

Timeline

20 May 2019Recall initiated by company
30 May 2019Classified by FDA+10 days
5 Jun 2019Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Firm has received complaints of finding pieces of glass in the products.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Suja Organic Kombucha - Mixed Berries: 15.2 oz. glass bottle; UPC 818617020362 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM

Where it was distributed

CA, NJ, GA, FL, NC, TX, IN, OH, MA, WI, CO, MI, VI, MN, PA, IA, NH, MD, IL, NY, MA

CaliforniaColoradoFloridaGeorgiaIowaIllinoisIndianaMassachusettsMarylandMichiganMinnesotaNorth CarolinaNew HampshireNew JerseyNew YorkOhioPennsylvaniaTexasWisconsin

Questions about this recall

Is Suja Organic Kombucha - Mixed Berries recalled?

Yes. Suja Life recalled Suja Organic Kombucha - Mixed Berries on 20 May 2019. The recall is Class II and its status is Terminated. Recall number F-1431-2019.

Why was it recalled?

Firm has received complaints of finding pieces of glass in the products.

Which lots are affected?

Best by 7/29/19

Where was it sold?

CA, NJ, GA, FL, NC, TX, IN, OH, MA, WI, CO, MI, VI, MN, PA, IA, NH, MD, IL, NY, MA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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