Wellnov recalls Liposomal Women's Liquid Multivitamin Drops (Iron Free) due to potential bacterial contamination and C. Botulinum concerns from manufacturing deviations. Affected units sold between Oct 2024 and Apr 2026.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Wellnov is recalling its Liposomal Women's Liquid Multivitamin Drops (Iron Free) because manufacturing issues could lead to bacterial contamination and potential C. Botulinum concerns. This affects products sold between October 2024 and April 2026.
The product was made using outdated Good Manufacturing Practices (cGMP) that could allow bacterial pathogens to grow. There is a potential risk of C. Botulinum, a serious foodborne pathogen that can cause food poisoning and neurological issues.
Women who purchased the Liposomal Women's Liquid Multivitamin Drops (Iron Free) between October 2024 and April 2026 are affected. Those with specific health conditions or compromised immune systems may be at higher risk.
Check for the product name 'Liposomal Women's Liquid Multivitamin Drops - Iron Free' on aluminum bottles. The lot number starts with WN0924 and was sold between October 2024 and April 2026.
Verify the product name, lot number (WN0924), and distribution dates (October 2024 to April 2026) to confirm if your item is affected.
The recall states that deviations from Good Manufacturing Practices could lead to bacterial pathogens and C. Botulinum concerns, but no specific safety status is provided.
Look for the product name 'Liposomal Women's Liquid Multivitamin Drops - Iron Free' on aluminum bottles with lot number WN0924 sold between October 2024 and April 2026.
The recall record does not specify a remedy, so no action steps are provided.
We’ve drafted a message you can send Wellnov to request your refund or repair — edit it as you like.
Subject: Recall H-0803-2026 — Wellnov Wellnov Hello, I own a Wellnov that is covered by recall H-0803-2026 from Wellnov. 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.
