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RECALL RECORD — CLASS IIIRecall closedF-0193-2020/FDA enforcement
Merical, LLC·Dietary Supplements·Oct 31, 2019

Leader Advanced Probiotic with 6 Probiotic Strains and 20 Billion Live Cultures

What you need to know

Class III

  • What happened

    Incorrect Probiotic blend indicated in the Supplemental Facts Panel on product label.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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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Match before you discard

Product identification

Source: FDA FOOD

Brand nameMerical, LLC
Recalling firmMerical, LLCOrange, CA, United States
UPC / barcodes
0 96295 13665 4
Lot / date codes
  • Batch Numbers: 300-00027721 and 300-00027515, Pkg Numbers: 907727721 and 913327515, Expiration Dates: 08/2020 and 04/2021.
Distribution area
Nationwide

One customer in OH who then distributed product nationwide

United States

Quantity affected442 cases
Recall initiationFDA report date: December 4, 2019
FDA recall numberF-0193-2020

Beyond the headline

The recall, in context

Merical, LLC initiated this supplements recall on October 31, 2019. The FDA enforcement report states: Incorrect Probiotic blend indicated in the Supplemental Facts Panel on product label. The FDA report lists distribution as: One customer in OH who then distributed product nationwide.

The FDA enforcement report describes the reason as: Incorrect Probiotic blend indicated in the Supplemental Facts Panel on product label.

Leader Advanced Probiotic with 6 Probiotic Strains and 20 Billion Live Cultures was made or distributed by Merical, LLC in Orange, CA, United States. This page reflects FDA report F-0193-2020, dated December 4, 2019.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 Leader Advanced Probiotic with 6 Probiotic Strains and 20 Billion Live Cultures recall?

Merical, LLC recalled Leader Advanced Probiotic with 6 Probiotic Strains and 20 Billion Live Cultures in an FDA Class III enforcement action reported as F-0193-2020. Incorrect Probiotic blend indicated in the Supplemental Facts Panel on product label.

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 Merical, LLC 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-0193-2020. 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.