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CPSC recall · Reported September 11, 2025

Blueroot Health Recalls Bottles of Bariatric Fusion Iron Multivitamins Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Manufactured by VitaQuest International

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-contain…

Recall #
25460
Affected scope
About 4,700
Compiled from official public sources by the editorial team.
Verify with CPSC →
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VitaQuest International, LLC of Caldwell, New Jersey recalled This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK … - a moderate-severity action.

Blueroot Health Recalls Bottles of Bariatric Fusion Iron Multivitamins Due to Risk of Ser… was recalled by VitaQuest International, LLC of Caldwell, New Jersey in September 11, 2025. Reason: The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poiso…. Remedy: Consumers should immediately secure the recalled bottles out of sight and reach of childr…. Verify recall #25460 with the CPSC before acting.

The recall

VitaQuest International, LLC of Caldwell, New Jersey issued this moderate-severity CPSC recall-The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poiso….

Moderate
severity level
September 11, 2025
reported

Sourced from official CPSC enforcement records. Verify recall #25460 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #25460) was formally reported on September 11, 2025. It is classified under Moderate severity, with a current status of Active. VitaQuest International, LLC of Caldwell, New Jersey is listed as the recalling firm. Federal records list the affected scope as About 4,700.

The documented reason for this recall is: 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 s… Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately secure the recalled bottles out of sight and reach of children, and contact Blueroot Health for information on how to obtain a free child-resistant replacement cap. - consumers holding this product should act on that instruction rather than relying on general guidance.

Within the same product category the archive holds 6 closely related recalls, 6 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,731 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 146
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

About 4,700

Related Recalls

6

6 from same agency

Product description

This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK multivitamin capsules (90 and 270-count bottles) and One Per Day bariatric multivitamin capsules (90-count bottle), both with 45mg of iron. The recalled bottles are white and orange. Only bottles with smooth cap tops that lack the "push down & turn" embossed lettering are included in this recall. The Bariatric Fusion logo is printed on the front of the bottles. Lot number 0066J4, 0065J4, 0453B5 or 0370B5 is printed on the bottom of the bottles.

Reason for recall

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 young children.

Remedy, what to do

Consumers should immediately secure the recalled bottles out of sight and reach of children, and contact Blueroot Health for information on how to obtain a free child-resistant replacement cap.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 25460
Date reported September 11, 2025
Date initiated September 11, 2025
Recalling firm VitaQuest International, LLC of Caldwell, New Jersey
Affected scope About 4,700
Distribution Not disclosed
Official source CPSC notice →

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

What to do with this recall

Consumers should immediately secure the recalled bottles out of sight and reach of children, and contact Blueroot Health for info…

  • Check the recall number (25460) and product description against the item you own. Search the archive
  • Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK multivitamin capsules (90 and 270-count bottles) and One Per Day bariatric multivitamin capsules (90-count bottle), both with 45mg of iron. The recalled bottles are white and orange. Only bottles with smooth cap tops that lack the "push down & turn" embossed lettering are included in this recall. The Bariatric Fusion logo is printed on the front of the bottles. Lot number 0066J4, 0065J4, 0453B5 or 0370B5 is printed on the bottom of the bottles.. Recalled by VitaQuest International, LLC of Caldwell, New Jersey. Units affected: About 4,700.
Why was this product recalled?
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 young children.
What should consumers do?
Consumers should immediately secure the recalled bottles out of sight and reach of children, and contact Blueroot Health for information on how to obtain a free child-resistant replacement cap.
Which agency issued this recall?
This recall was issued by the CPSC on September 11, 2025. Severity: Moderate. Recall number: 25460.
How do I check if my product is affected by a recall?
Check the product description and recall number (25460) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported September 11, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.