Check the Batch
Class IITerminated in FDA datasetRecall initiated May 20, 2019

Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of Ginger Lemon, Mixes…

Recalling firm: Suja Life LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 20, 2019.

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Compare the exact product and package details with the label you have.

ProductSuja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of Ginger Lemon, Mixes Berries and Peach Ginger UPC 818617020737; DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM
Package size15.2 oz
UPC818617020737

FDA code information

Best by 7/29/19, 7/28/19, 7/27/19, 6/28/19, 6/27/19, 6/25/19, 6/12/19, 6/8/19, 6/7/19, and 6/6/19.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of Ginger Lemon, Mixes Berries and Peach Ginger UPC 818617020737; DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM

Extracted codes and context

TypeCode / valueContext
UPC818617020737 oz. glass bottle; 2 each of Ginger Lemon, Mixes Berries and Peach Ginger UPC 818617020737; DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM
best by7/29/19Best by 7/29/19, 7/28/19, 7/27/19, 6/28/19, 6/27/19, 6/25/19, 6/12/19, 6/8/19, 6/7/19, and 6/6/19.

Original FDA recall reason

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

Recall details

Recall number
F-1432-2019
Event ID
82898
FDA status
Terminated
Initiated
May 20, 2019
Reported
Jun 5, 2019
Classified
May 30, 2019
Terminated
Aug 20, 2019
Quantity
31,079 cases
Location
San Diego, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

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

FDA source record · F-1432-2019

Data updated September 16, 2026. View official FDA data ↗

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