Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per
Summary
The FDA issued a Class II for Food Research International - Uro Kid Support Capsules, packaged in glass bottle by Global Vitality Inc.. Reason: potential contamination with E coli.
Details
Source
Food Recall
External ID
F-1442-2023
Action Date
2023-08-23
Status
Ongoing
Category
food
Product Description
Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
Lot/Code Info: Item # B6517 Lot #9237 Product # DRR6517-90VC Best By 01/26
Quantity Affected: 2975 bottles total
Reason for Recall
potential contamination with E coli
Distribution
Distributed to single consignee in California
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-13
Company
Chandler, AZ
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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Global Vitality Inc. has 2 FDA actions in our database, including 2 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 (Global Vitality Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Global Vitality Inc. have FDA actions?
Global Vitality Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1442-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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