Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray... — FDA record F-0358-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 1, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray affected area 2-5 times daily as needed. 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 Livia Global Inc., Visalia, CA.
Reason
Probiotic products contaminated with Pseudomonas aeruginosa .
Classification
Class II
Recalling firm
Livia Global
Quantity
571 bottles
Agency-reported status
Terminated
Source record identifier
F-0358-2022

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What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot #001005-1, BB 04/2023

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

xx

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Report date
Dec 22, 2021
Recall initiation date
Dec 1, 2021
Center classification date
Jan 2, 2022
Termination date
Apr 29, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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