Class IIITerminated in FDA datasetRecall initiated Oct 31, 2019

Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Live Cultures. 30 capsules…

Recalling firm: Merical, LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 6, 2020.

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ProductLeader Advanced Probiotic with 6 Probiotic Strains and 20 billion Live Cultures. 30 capsules Item Number: CARD40359, Product Number: 907019, UPC Code: 096295136654
UPC096295136654

FDA code information

Batch Numbers: 300-00027721 and 300-00027515, Pkg Numbers: 907727721 and 913327515, Expiration Dates: 08/2020 and 04/2021.

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Full FDA record and distribution details

Original product description

Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Live Cultures. 30 capsules Item Number: CARD40359, Product Number: 907019, UPC Code: 096295136654

Extracted codes and context

TypeCode / valueContext
UPC096295136654tures. 30 capsules Item Number: CARD40359, Product Number: 907019, UPC Code: 096295136654

Original FDA recall reason

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

Recall details

Recall number
F-0193-2020
Event ID
84302
FDA status
Terminated
Initiated
Oct 31, 2019
Reported
Dec 4, 2019
Classified
Nov 26, 2019
Terminated
Mar 6, 2020
Quantity
442 cases
Location
Orange, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

One customer in OH who then distributed product nationwide

FDA source record · F-0193-2020

Data updated September 16, 2026. View official FDA data ↗

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