FDA recall record
Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) UPC: 0 30915 10711 2 - 2 oz. 0 30915 10716 7 - 4 oz. Recommended use: Internal: Adult...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 29, 2022. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) UPC: 0 30915 10711 2 - 2 oz. 0 30915 10716 7 - 4 oz. Recommended use: Internal: Adults 4 droppers full daily. Children 12 yrs and under 1-2 droppers daily. Ingredients: Proprietary probiotic blend in an enzyme enriched substrate: Lactobacillus-Acidophilus, L. Rhamnosus, L-Salivarius, L.
Casei, L-Plantarum, Lactococcus-Lactis, Streptocuccus-Thermophilus, Bifidobacterium-Bifidum, B-Lactus, B-Infantis, B-Breve, B-Longum. Made with water and a proprietary blend of three organic grasses.
Reason
Probiotic products contaminated with Pseudomonas aeruginosa .
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) UPC: 0 30915 10711 2 - 2 oz. 0 30915 10716 7 - 4 oz. Recommended use: Internal: Adults 4 droppers full daily. Children 12 yrs and under 1-2 droppers daily. Ingredients: Proprietary probiotic blend in an enzyme enriched substrate: Lactobacillus-Acidophilus, L. Rhamnosus, L-Salivarius, L.
Casei, L-Plantarum, Lactococcus-Lactis, Streptocuccus-Thermophilus, Bifidobacterium-Bifidum, B-Lactus, B-Infantis, B-Breve, B-Longum. Made with water and a proprietary blend of three organic grasses.
Code information listed by FDA
Lot #001005-1, BB 04/2023
Distribution and firm information
Recalling firm listed by FDA: Livia Global
Firm location listed by FDA: Visalia, CA, United States
Distribution reported by FDA: xx
Product quantity listed by FDA: 1067 x 2 oz. bottles, 384 x 4 oz. bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.