Exact FDA event identifier

Event 88956

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: October 28, 2021
Product types: Food
Classifications: Class I
Statuses: Terminated
Recalling firm wording: MARY RUTH ORGANICS

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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.

F-0214-2022

Recall number: F-0214-2022
Initiated: October 28, 2021
Classification: Class I
Status: Terminated
Recalling firm: MARY RUTH ORGANICS
Quantity: Lot# 100420218 = 23,223 Lot# 100520218 = 2,450

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

found the presence of Pseudomonas

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

Nationwide distribution