CLASS II Food recall · Reported 22 Dec 2021 · FDA Enforcement Report

Livia One Organic Daily Topical Spray Probiotics recalled

Livia Global is recalling Livia One Organic Daily Topical Spray Probiotics. The recall was initiated on 1 Dec 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #001005-1, BB 04/2023
Quantity recalled571 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0358-2022
FDA event ID
89115
Recalling firm
Livia Global, Visalia, CA
Classification
Class II
Status
Terminated
Recall initiated
1 Dec 2021
FDA classified
2 Jan 2022
Reported
22 Dec 2021
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Sterility
Product category
Probiotics

Timeline

1 Dec 2021Recall initiated by company
22 Dec 2021Published in enforcement report+21 days
2 Jan 2022Classified by FDA+11 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Probiotic products contaminated with Pseudomonas aeruginosa .

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

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.

Where it was distributed

xx

Questions about this recall

Why was it recalled?

Probiotic products contaminated with Pseudomonas aeruginosa .

Which lots are affected?

Lot #001005-1, BB 04/2023

Where was it sold?

xx

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 89115

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