Suja Life LLC
Complete recall history across all FDA and CPSC categories — 8 total recalls
Suja Life LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Food Recalls (8)
FDA food safety enforcement actions by Suja Life LLC
| Date | Product | Reason | Class |
|---|---|---|---|
| Feb 13, 2020 | Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234 | Firm was notified by supplier of an unapproved herbicide in raw material, fla... | Class II |
| Feb 13, 2020 | Suja Organic Mango Mojito Fruit + Veggie Smoothie, 12 oz. UPC: 81861702240 | Firm was notified by supplier of an unapproved herbicide in raw material, fla... | Class II |
| Feb 13, 2020 | Suja Organic Tropical Dragon Fruit + Veggie Smoothie, 12 oz. UPC: 81861702238 | Firm was notified by supplier of an unapproved herbicide in raw material, fla... | Class II |
| Feb 13, 2020 | Suja Organic Ginger Bliss Fruit + Veggie Smoothie, 12 oz. UPC: 81861702236 | Firm was notified by supplier of an unapproved herbicide in raw material, fla... | Class II |
| May 20, 2019 | Suja Organic Kombucha - Mixed Berries: 15.2 oz. glass bottle; UPC 818617020... | Firm has received complaints of finding pieces of glass in the products. | Class II |
| May 20, 2019 | Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of ... | Firm has received complaints of finding pieces of glass in the products. | Class II |
| May 20, 2019 | Suja Organic Kombucha - Peach Ginger: 15.2 oz. glass bottle; UPC 8186170203... | Firm has received complaints of finding pieces of glass in the products. | Class II |
| May 20, 2019 | Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 8186170202... | Firm has received complaints of finding pieces of glass in the products. | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
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