DNE Nutraceuticals recalls Adwe Naturals Prenatal Vitamins due to potential folic acid potency issues. Learn if you have the affected product and what to do.
Adwe Prenatal tablets are being recalled due to a concern of potency of folic acid.
DNE Nutraceuticals is recalling Adwe Naturals Prenatal Vitamins because of concerns about folic acid potency. This could affect pregnant women and those who take prenatal supplements, though the recall does not indicate immediate health risks.
The recall is due to concerns that the folic acid in these prenatal vitamins may not be as potent as intended. This could potentially lead to inadequate folic acid intake for pregnant women, though the product does not pose an immediate health risk.
Pregnant women and others who take Adwe Naturals Prenatal Vitamins are likely affected. The risk is lowest for those who do not take the product regularly.
Check for the UPC 040168805079 on the product label. The product was manufactured for Adwe Laboratories in Brooklyn, NY, and has lot number 8990.
Look for the UPC 040168805079 and lot number 8990 on the product label.
The recall is due to concerns about folic acid potency, but the product does not pose an immediate health risk. Consult your healthcare provider for personalized advice.
Check for the UPC 040168805079 and lot number 8990 on the product label.
The recall does not specify a remedy, so contact DNE Nutraceuticals for guidance.
We’ve drafted a message you can send Adwe Naturals to request your refund or repair — edit it as you like.
Subject: Recall F-0190-2017 — Adwe Naturals Adwe Naturals Hello, I own a Adwe Naturals that is covered by recall F-0190-2017 from Adwe 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
