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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Food
Medications & Supplements/Dietary Supplements

Livia Global: Probiotic Liquids, Sprays, and Nasal Sprays Recalled for Bacterial Contamination

Agency Publication Date: December 13, 2021
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Summary

Livia Global is recalling 2,768 units of its Livia One Organic probiotic products, including daily liquid probiotics, topical sprays, and nasal sprays, because they may be contaminated with Pseudomonas aeruginosa. This bacteria was discovered during routine testing of the affected lots. Consumers should immediately stop using these products and return them to the place of purchase for a full refund.

Risk

Pseudomonas aeruginosa is a bacterium that can cause serious infections, particularly in individuals with weakened immune systems or those using the product on sensitive areas like the nasal passages. Infections from this bacteria can be difficult to treat and may lead to severe health complications if it enters the bloodstream or lungs.

What You Should Do

  1. Check your product packaging for the following identifying lot numbers: Lot #001005-1 (Best By 04/2023) or Lot #010620-1 (Best By 08/2023).
  2. Verify the UPC codes on your bottles: Livia One Daily Liquid Probiotics 2 oz (0 30915 10711 2) and 4 oz (0 30915 10716 7); Topical Spray 4 oz (0 30915 10710 5); or Nasal Spray 1 oz (0 30915 10719 8).
  3. Immediately stop using any of the affected products listed above to avoid the risk of bacterial infection.
  4. Return the affected product to the store or place of purchase where it was bought to receive a full refund.
  5. If you have used these products and are experiencing unusual symptoms, contact your healthcare provider or pharmacist for guidance.
  6. For further information or questions regarding this recall, contact Livia Global directly or call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund for returned products.

How to: Return to the place of purchase for a full refund or contact the manufacturer for further instructions.

Affected Products

Product: Livia One Organic Daily Liquid Probiotics (2 oz. / 59 ml)
Item Code:
F-0357-2022
UPC Codes:
030915107112
Lot Numbers:
001005-1 (BB 04/2023)
Date Ranges: Best By 04/2023
Product: Livia One Organic Daily Liquid Probiotics (4 oz. / 120 ml)
Item Code:
F-0357-2022
UPC Codes:
030915107167
Lot Numbers:
001005-1 (BB 04/2023)
Date Ranges: Best By 04/2023
Product: Livia One Organic Daily Topical Spray Probiotics (4 oz. / 120 ml)
Item Code:
F-0358-2022
UPC Codes:
030915107105
Lot Numbers:
001005-1 (BB 04/2023)
Date Ranges: Best By 04/2023
Product: Livia One Organic Probiotic Nasal Spray (1 oz. / 30 ml)
Item Code:
F-0359-2022
UPC Codes:
030915107198
Lot Numbers:
001005-1 (BB 04/2023)
010620-1 (BB 08/2023)
Date Ranges: Best By 04/2023, Best By 08/2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89115
Status: Resolved
Manufacturer: Livia Global
Manufactured In: United States
Units Affected: 3 products (1067 x 2 oz. bottles, 384 x 4 oz. bottles; 571 bottles; 1130 x 1 oz. bottles)
Distributed To: Nationwide
Agency Last Updated: January 2, 2022

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.