PlainRecalls

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

Reported: September 11, 2025 Initiated: September 11, 2025 #25460 About 4,700 units

VitaQuest International, LLC of Caldwell, New Jersey issued this CPSC recall on September 11, 2025. Classified as Moderate severity. Approximately About 4,700 units are affected. The recall was issued because: The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poison Preventi…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

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 indicate About 4,700 units are affected.

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.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 1 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 1 year old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 4,700

Related Recalls

6

1 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

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
Units affected About 4,700
Distribution Not disclosed

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

Scale of Impact

About 4,700 units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

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.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, … →

Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).