Natural Systems, Naturasys MULTI VITAMIN HIGH POTENCY AND FORMULATION, Dietary Supplement 60 Tablets
Summary
The FDA issued a Class III for Natural Systems, Naturasys MULTI VITAMIN HIGH POTENCY AND FORMULATION, Dietary S by Emceta International Inc.. Reason: FDA sample analysis of Natural Systems brand Multi Vitamin, 60 Tablets, found the magnesium content as 33.5% of the amount declared in label..
Details
Source
Food Recall
External ID
F-1295-2023
Action Date
2023-08-02
Status
Terminated
Category
food
Product Description
Natural Systems, Naturasys MULTI VITAMIN HIGH POTENCY AND FORMULATION, Dietary Supplement 60 Tablets
Lot/Code Info: Lot 38883, Exp. 07/2024
Quantity Affected: 554 bottles/60 tablets each
Reason for Recall
FDA sample analysis of Natural Systems brand Multi Vitamin, 60 Tablets, found the magnesium content as 33.5% of the amount declared in label.
Distribution
Domestic and Foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-10
Company
Doral, FL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Emceta International Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Emceta International Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Emceta International Inc. have FDA actions?
Emceta International 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-1295-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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