Magno Humphries recalls gluten-free vitamin E supplement with 1000 IU per softgel due to labeling error. Product contains 100 softgels in white HDPE bottle with foil cap. No action needed as it's a labeling discrepancy.
Magno Humphries Laboratories is recalling Vitamin E softgels because the principle display panel states the product contains 1000 IU of Vitamin E however the Supplement Facts label indicated 200 IU of Vitamin E. The supplement actually contains 1000 IU of Vitamin E.
Magno Humphries is recalling their gluten-free vitamin E supplement because the product actually contains 1000 IU of Vitamin E, but the label incorrectly states 200 IU. This is a labeling error, not a safety hazard.
The product contains 1000 IU of Vitamin E instead of the labeled 200 IU. This is a labeling error, not a safety hazard. The supplement is gluten-free but may have cross-contamination risks for people with celiac disease.
People who purchased the gluten-free vitamin E supplement from retailers like Walmart, Target, or online. Those with celiac disease or gluten sensitivity are most at risk due to potential cross-contamination.
Look for the product in a white HDPE bottle with a foil cap. It contains 100 softgels and has UPCs 043292562917, 343230, 343695, 343788, 344603, or 344936.
Verify the Supplement Facts label shows 200 IU of Vitamin E, but the product contains 1000 IU.
Yes, the product is safe to use. This recall is due to a labeling error, not a safety hazard.
No, you do not need to stop using this product. It is a labeling error, not a safety hazard.
Look for the product in a white HDPE bottle with a foil cap. It contains 100 softgels and has UPCs 043292562917, 343230, 343695, 343788, 344603, or 344936.
We’ve drafted a message you can send Magno Humphries to request your refund or repair — edit it as you like.
Subject: Recall F-1821-2014 — Magno Humphries Magno Humphries Hello, I own a Magno Humphries that is covered by recall F-1821-2014 from Magno Humphries. 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.
