RecallHawk

Bariatric Fusion Iron Multivitamin Bottles

VitaQuest International, LLC of Caldwell, New Jersey

Summary

CPSC recall: Bariatric Fusion Iron Multivitamin Bottles. By VitaQuest International, LLC of Caldwell, New Jersey. Hazard: The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The recalled packaging of the iron-containing multivitamins violates the federal standard for child-resistant packaging because the bottle caps are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by youn

Details

Source

CPSC Consumer Product Recall

External ID

10400

Action Date

2025-09-11

Status

Recalled

Category

consumer_product

Product Description

This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK multivitamin capsules (90 and 2

Context & Analysis

This is a unclassified recall.

This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

VitaQuest International, LLC of Caldwell, New Jersey has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA 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 (VitaQuest International, LLC of Caldwell, New Jersey) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does VitaQuest International, LLC of Caldwell, New Jersey have FDA actions?

VitaQuest International, LLC of Caldwell, New Jersey has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10400" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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