Livia Global — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Livia Global has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 1 Dec 2021. Livia Global is categorized under Beverages based on their predominant recall history.
Recall activity over time for Livia Global
How serious are Livia Global recalls?
FDA recall classifications by severity
Full FDA recall history for Livia Global
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 1 Dec 2021Official FDA Notice | Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: S | Probiotic products contaminated with Pseudomonas aeruginosa . | Class IITerminated |
| 1 Dec 2021Official FDA Notice | Livia One Organic Probiotic Nasal Spray; 1 oz. (30 ml) UPC: 0 30915 10719 8 Suggested use: Adult – 102 pumps in e | Probiotic products contaminated with Pseudomonas aeruginosa . | Class IITerminated |
| 1 Dec 2021Official FDA Notice | Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) UPC: 0 30915 10711 2 – 2 oz. 0 | Probiotic products contaminated with Pseudomonas aeruginosa . | Class IITerminated |
Where have Livia Global recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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