FDA recall record

Livia One Organic Daily Topical Spray Probiotics recall — FDA F-0358-2022

Probiotic products contaminated with Pseudomonas aeruginosa .

Class IIclassification
F-0358-2022official record ID
Dec 22, 2021report date

Recall record at a glance

Official recordF-0358-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLivia Global
Report dateDec 22, 2021
Recall initiation dateDec 1, 2021
Quantity571 bottles
LocationVisalia, CA, United States

Official product description

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.

Why the product was recalled

Probiotic products contaminated with Pseudomonas aeruginosa .

Distribution information

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How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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