Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of Ginger Lemon, Mixes Berries and Peach Ginger
Recalling firm: Suja Life LLC
Why it was recalled
Firm has received complaints of finding pieces of glass in the products.
Check your package
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
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
| Type | Code / value | Context |
|---|---|---|
| UPC | 818617020737 | 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 by | 7/29/19 | 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. |
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 ↗
Follow official FDA and manufacturer guidance.