Class ITerminated in FDA datasetOct 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.

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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.
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

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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