Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: S
Summary
The FDA issued a Class II for Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 by Livia Global. Reason: Probiotic products contaminated with Pseudomonas aeruginosa ..
Details
Source
Food Recall
External ID
F-0358-2022
Action Date
2021-12-22
Status
Terminated
Category
food
Product Description
Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray affected area 2-5 times daily as needed. Ingredients: Proprietary probiotic blend in an enzyme enriched substrate: Lactobacillus-Acidophilus, L. Rhamnosus, L-Salivarius, L. Casei, L-Plantarum, Lactococcus-Lactis, Streptocuccus-Thermophilus, Bifidobacterium-Bifidum, B-Lactus, B-Infantis, B-Breve, B-Longum. Made with water and a proprietary blend of three organic grasses Livia Global Inc., Visalia, CA.
Lot/Code Info: Lot #001005-1, BB 04/2023
Quantity Affected: 571 bottles
Reason for Recall
Probiotic products contaminated with Pseudomonas aeruginosa .
Distribution
xx
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-01
Company
Visalia, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Livia Global has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Livia Global) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Livia Global have FDA actions?
Livia Global has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0358-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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