ActiPharma recalls ACTIRON Dietary Supplement (Lot 13309, Exp: 01/26) due to folic acid levels not matching label claims. Consumers should check product details and contact the company for guidance.
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
ActiPharma is recalling ACTIRON Dietary Supplements that may not contain the labeled amount of folic acid. This could affect users who need proper folic acid intake, especially pregnant individuals or those with specific medical conditions.
The product failed FDA testing for folic acid content compared to its label claim. This means the supplement might not provide the intended nutritional benefit, which could be important for certain health needs.
Pregnant women and individuals with medical conditions requiring folic acid may be at higher risk due to potential inadequate nutrient levels. Most consumers are unlikely to experience serious harm from this issue.
Check for the product name 'ACTIRON Dietary Supplement', 100 tablets, Lot 13309, with expiration date 01/26. The UPC code 363102217104 is also associated with this specific batch.
Look for the lot number 13309 and expiration date 01/26 on the packaging.
The product may not contain the labeled amount of folic acid, but it is not considered dangerous. Consumers should check if they have the recalled batch and contact ActiPharma for guidance.
The recall does not specify a remedy, so you should check the product details and contact ActiPharma for further instructions.
Check for the lot number 13309 and expiration date 01/26 on the packaging, or the UPC code 363102217104.
We’ve drafted a message you can send ActiPharma to request your refund or repair — edit it as you like.
Subject: Recall F-0463-2024 — ActiPharma ActiPharma Hello, I own a ActiPharma that is covered by recall F-0463-2024 from ActiPharma. 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.
