Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 1, 2021 (5 years ago)

Livia One Organic Daily Liquid Probiotics recall

Recalled by Livia Global · Visalia, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Probiotic products contaminated with Pseudomonas aeruginosa .

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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.

Quantity: 1067 x 2 oz. bottles, 384 x 4 oz. bottles

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot #001005-1, BB 04/2023

Where it was sold

FDA's distribution note: xx

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Livia Global
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 1, 2021
In FDA report of
Dec 22, 2021
Terminated
Apr 29, 2022
FDA recall number
F-0357-2022 · event 89115
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.