FDA recall record
Livia One Organic Probiotic Nasal Spray; 1 oz. (30 ml) UPC: 0 30915 10719 8 Suggested use: Adult - 102 pumps in each nostril as needed 1-3 times per day; Children 4-12 y...
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 Probiotic Nasal Spray; 1 oz. (30 ml) UPC: 0 30915 10719 8 Suggested use: Adult - 102 pumps in each nostril as needed 1-3 times per day; Children 4-12 years : 1/4-1/2 pump in each nostril as needed - 103 times daily as needed. Children 3 and under: It is always advised to consult with a pediatrician or healthcare provided before use..
Ingredients: Proprietary probiotic blend in an enzyme enriched substrate. , Visalia, CA.
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 Probiotic Nasal Spray; 1 oz. (30 ml) UPC: 0 30915 10719 8 Suggested use: Adult - 102 pumps in each nostril as needed 1-3 times per day; Children 4-12 years : 1/4-1/2 pump in each nostril as needed - 103 times daily as needed. Children 3 and under: It is always advised to consult with a pediatrician or healthcare provided before use..
Ingredients: Proprietary probiotic blend in an enzyme enriched substrate. , Visalia, CA.
Code information listed by FDA
Lot #001005-1, BB 04/2023; Lot # 010620-1, BB 08/2023
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: 1130 x 1 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.