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Class ITerminated in FDA datasetRecall initiated Oct 28, 2021

MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL)

Recalling firm: MARY RUTH ORGANICS

Why it was recalled

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

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: Feb 18, 2022.

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Compare the exact product and package details with the label you have.

ProductMaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7 Serving size (five drops - start with one and work up to 5) Organic Proprietary Probiotic Blend 250 mg. Bifidobacterium lactis Bifidobacterium infantis Bifidobacterium bifidum Lactobacillus reuteri Other ingredients: A blend of probiotics in an enzyme enriched substrate, extracted with water from a proprietary blend of three organic grasses.
Package size1 fl. oz
UPC856645008587

FDA code information

lots: 100420218, expiry 4/2023 and 100520218, expiry 5/2023

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Full FDA record and distribution details

Original product description

MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7 Serving size (five drops - start with one and work up to 5) Organic Proprietary Probiotic Blend 250 mg. Bifidobacterium lactis Bifidobacterium infantis Bifidobacterium bifidum Lactobacillus reuteri Other ingredients: A blend of probiotics in an enzyme enriched substrate, extracted with water from a proprietary blend of three organic grasses.

Extracted codes and context

TypeCode / valueContext
UPC856645008587s Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7 Serving size (five drops - start with one and work up to 5) Organic Proprietary Probiotic Blend 250 mg. Bifidobact

Original FDA recall reason

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

Recall details

Recall number
F-0214-2022
Event ID
88956
FDA status
Terminated
Initiated
Oct 28, 2021
Reported
Dec 1, 2021
Classified
Nov 19, 2021
Terminated
Feb 18, 2022
Quantity
Lot# 100420218 = 23,223 Lot# 100520218 = 2,450
Location
Los Angeles, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide distribution

FDA source record · F-0214-2022

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

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