09/11/2025 | Press release | Distributed by Public on 09/11/2025 07:24
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.
About 4,700
Blueroot Health toll-free at 866-259-0602 from 8 a.m. to 6 p.m. ET Monday through Friday, email at [email protected], or online at bariatricfusion.com/product-safetyor https://www.bariatricfusion.comand click "Recall" at the bottom of the page for more information.
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.
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.
None reported
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.
The bottles contain turpentine, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are ingested by young children.
The recalled bottles contain turpentine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The turpentine bottles violate the mandatory standard for child-resistant packaging, posing a deadly poisoning hazard to young children.
The lid can forcefully eject, posing serious impact and laceration hazards, when a consumer attempts to open the capped bottles after food, carbonated beverages or perishable beverages, such as juice or milk, are stored inside over time.
The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The iron-containing dietary supplement packages violate the federal standard for child-resistant packaging because the bottles and blister packs are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.
The Safetussin over-the-counter cold medicine contains acetaminophen, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the products is not child-resistant as a tablet can be pushed through the foil, posing a risk of poisoning if the contents are swallowed by young children.
The U.S. Consumer Product Safety Commission (CPSC) is charged with protecting the public from unreasonable risk of injury associated with the use of thousands of types of consumer products. Deaths, injuries, and property damage from consumer product-related incidents cost the nation more than $1 trillion annually. Since the CPSC was established more than 50 years ago, it has worked to ensure the safety of consumer products, which has contributed to a decline in injuries associated with these products.
Federal law prohibits any person from selling products subject to a Commission ordered recall or a voluntary recall undertaken in consultation with the CPSC.
For lifesaving information: