RECALL RECORD — CLASS IRecall closedF-0214-2022/FDA enforcement

Maryruth's Organic Infants Liquid Probiotic

What you need to know

Class I
  • What happened

    Internal testing found the presence of Pseudomonas aeruginosa in the product.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. 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 FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameMary Ruth Organics
Recalling firmMary Ruth OrganicsLos Angeles, CA, United States
UPC / barcodes
8 56645 00858 7
Lot / date codes
  • lots: 100420218, expiry 4/2023 and 100520218, expiry 5/2023
Distribution area
Nationwide

Nationwide distribution

United States

Quantity affectedLot# 100420218 = 23, 223 Lot# 100520218 = 2, 450
Recall initiationFDA report date: December 1, 2021
FDA recall numberF-0214-2022

Beyond the headline

The recall, in context

Mary Ruth Organics initiated this supplements recall on October 28, 2021. The FDA enforcement report states: Internal testing found the presence of Pseudomonas aeruginosa in the product. The FDA report lists distribution as: Nationwide distribution.

The FDA enforcement report describes the reason as: Internal testing found the presence of Pseudomonas aeruginosa in the product.

Maryruth's Organic Infants Liquid Probiotic was made or distributed by Mary Ruth Organics in Los Angeles, CA, United States. This page reflects FDA report F-0214-2022, dated December 1, 2021.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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 Maryruth's Organic Infants Liquid Probiotic recall?

Mary Ruth Organics recalled Maryruth's Organic Infants Liquid Probiotic in an FDA Class I enforcement action reported as F-0214-2022. Internal testing found the presence of Pseudomonas aeruginosa in the product.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Mary Ruth Organics?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0214-2022 and keep the packaging, lot code and proof of purchase if you have them.

Is the Mary Ruth Organics 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-0214-2022. 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

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