Source Naturals recalls hydrogen boost capsules due to low levels of undeclared boron. Consumers should check product lot numbers and contact the company for details.
Dietary supplements contain low levels of undeclared boron
Source Naturals is recalling hydrogen boost capsules that contain low levels of undeclared boron. This could pose a risk for people who take dietary supplements regularly, though the levels are not high enough to cause serious harm.
The capsules contain low levels of boron that were not declared on the label. Boron is a mineral that can be harmful in high doses, but the levels in these supplements are low and unlikely to cause serious health issues.
People who have purchased Source Naturals Hydrogen Boost capsules (6-count trial, 30-count, or 60-count bottles) are affected. Those who take dietary supplements daily may be at slightly higher risk due to boron exposure.
Check the product label for the brand 'Source Naturals Hydrogen Boost' and the lot numbers listed in the recall (e.g., FG-49254, FG-20141, etc.). The capsules come in 6-count trial, 30-count, or 60-count bottles.
Look for the lot numbers listed in the recall (e.g., FG-49254, FG-20141) on the product label.
The recall states that the capsules contain low levels of undeclared boron, which is unlikely to cause serious health issues. However, the product is being recalled for transparency and potential regulatory compliance.
Check the product label for lot numbers like FG-49254, FG-20141, or others listed in the recall details. The product comes in 6-count trial, 30-count, or 60-count bottles.
The recall does not specify a remedy, so consumers should check the product label for lot numbers and contact Source Naturals for further instructions.
We’ve drafted a message you can send Source Naturals to request your refund or repair — edit it as you like.
Subject: Recall F-2380-2017 — Source Naturals Source Naturals Hello, I own a Source Naturals that is covered by recall F-2380-2017 from Source Naturals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
