MARY RUTH ORGANICS Recall: Internal testing found the presence of Pseudomonas aeruginosa in the product. - F-0214-2022
United States
TerminatedClass I
- Company
- MARY RUTH ORGANICS
- Product
- MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a…
- Recall date
- October 28, 2021
- Terminated
- February 18, 2022
- Source
- FDA
Reason for recall
Internal testing found the presence of Pseudomonas aeruginosa in the product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | Lot# 100420218 = 23,223 Lot# 100520218 = 2,450 | lots: 100420218, expiry 4/2023 and 100520218, expiry 5/2023 |
Distribution
- Nationwide distribution
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0214-2022
- Event ID
- 88956
- Status
- Terminated
- Classification
- Class I
- Company
- MARY RUTH ORGANICS
- 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.
- Quantity
- Lot# 100420218 = 23,223 Lot# 100520218 = 2,450
- Reason
- Internal testing found the presence of Pseudomonas aeruginosa in the product.
- Recall initiation date
- October 28, 2021
- Report date
- December 1, 2021
- Classification date
- Not published in this source record
- Termination date
- February 18, 2022
- Distribution pattern
- Nationwide distribution
- UPC, lot, and code information
- lots: 100420218, expiry 4/2023 and 100520218, expiry 5/2023
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: MARY RUTH ORGANICS
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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Technical source data
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Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of February 18, 2022.
Status as reported: Terminated.
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