---
title: "Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) U... — FDA record F-0357-2022 | Is It on Recall"
description: "Probiotic products contaminated with Pseudomonas aeruginosa ."
url: https://isitonrecall.com/recall/fda-food-f-0357-2022-livia-one-organic-daily-liquid-probiotics-2-oz-59-ml-and-4-oz-120-ml-upc-0-30915-10711-2-2-oz-0-3091/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Livia One Organic Daily Liquid Probiotics; 2 oz. (59 ml) and 4 oz. (120 ml) UPC: 0 30915 10711 2 - 2 oz. 0 30915 1071... — FDA record F-0357-2022

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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.
- **Reason**: Probiotic products contaminated with Pseudomonas aeruginosa .
- **Classification**: Class II
- **Recalling firm**: Livia Global
- **Quantity**: 1067 x 2 oz. bottles, 384 x 4 oz. bottles
- **Agency-reported status**: Terminated
- **Source record identifier**: F-0357-2022

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0357-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot #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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0357-2022%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [Livia Global records](https://isitonrecall.com/brand/livia-global/)