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RECALL RECORD — CLASS IIRecall closedF-0357-2022/FDA enforcement
Livia Global·Dietary Supplements·Dec 1, 2021

Livia One Organic Daily Liquid Probiotics

What you need to know

Class II

  • What happened

    Probiotic products contaminated with Pseudomonas aeruginosa.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameLivia Global
Recalling firmLivia GlobalVisalia, CA, United States
UPC / barcodes
0 30915 10711 20 30915 10716 7
Lot / date codes
  • Lot #001005-1, BB 04/2023
Distribution area

xx

United States

Quantity affected1067 x 2 oz. bottles, 384 x 4 oz. bottles
Recall initiationFDA report date: December 22, 2021
FDA recall numberF-0357-2022

Beyond the headline

The recall, in context

Livia Global initiated this supplements recall on December 1, 2021. The FDA enforcement report states: Probiotic products contaminated with Pseudomonas aeruginosa. The FDA report lists distribution as: xx.

The FDA enforcement report describes the reason as: Probiotic products contaminated with Pseudomonas aeruginosa.

Livia One Organic Daily Liquid Probiotics was made or distributed by Livia Global in Visalia, CA, United States. This page reflects FDA report F-0357-2022, dated December 22, 2021.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Livia One Organic Daily Liquid Probiotics recall?

Livia Global recalled Livia One Organic Daily Liquid Probiotics in an FDA Class II enforcement action reported as F-0357-2022. Probiotic products contaminated with Pseudomonas aeruginosa.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Livia Global recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0357-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Livia Global

View brand
Class II·

Livia Global

Livia One Organic Daily Topical Spray Probiotics

Probiotic products contaminated with Pseudomonas aeruginosa.

Distribution not listedSupplements
Class II·

Livia Global

Livia One Organic Probiotic Nasal Spray

Probiotic products contaminated with Pseudomonas aeruginosa.

Distribution not listedSupplements

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.