RecallHawk
Class III Recall

Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets

Mason Vitamins, Inc.

Summary

The FDA issued a Class III for Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets by Mason Vitamins, Inc.. Reason: Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims..

Details

Source

Food Recall

External ID

F-0425-2023

Action Date

2023-03-22

Status

Terminated

Category

food

Product Description

Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets

Lot/Code Info: Lot No./Expiration Date: - 25807G/9-24 and 25222G/7-24

Quantity Affected: 37,330 bottles/ 20 tablets ea

Reason for Recall

Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-11-14

Company

Mason Vitamins, Inc.

Miami Lakes, 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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Mason Vitamins, 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 (Mason Vitamins, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mason Vitamins, Inc. have FDA actions?

Mason Vitamins, 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-0425-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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