Wellnov recalls Liposomal Women's 50+ Liquid Multivitamin Drops (90ml aluminum bottles) manufactured between Oct 2024 and Apr 2026 due to potential bacterial contamination and C. Botulinum concerns. Consumers should check lot numbers.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Wellnov is recalling Liposomal Women's 50+ Liquid Multivitamin Drops because of possible bacterial contamination and concerns about C. Botulinum. This could lead to foodborne illness if the product is consumed.
The product was made using Good Manufacturing Practices that deviated from standards, potentially allowing bacterial pathogens to grow. There are also concerns about C. Botulinum, a dangerous bacteria that can cause serious illness.
Women aged 50 and older who purchased the Liposomal Women's 50+ Liquid Multivitamin Drops between October 2024 and April 2026 are affected. Those with compromised immune systems may be at higher risk.
Check for aluminum bottles labeled 'Liposomal Womens 50+ Liquid Multivitamin Drops' with a lot number starting with 'W+0925' and an expiration date of September 2027. The product was distributed from October 2024 to April 2026.
Look for the lot number starting with 'W+0925' and expiration date of September 2027 on the aluminum bottle.
The recall states there are concerns about bacterial pathogens and C. Botulinum, but no specific safety advice is given for use.
Check for aluminum bottles labeled 'Liposomal Womens 50+ Liquid Multivitamin Drops' with lot number starting with 'W+0925' and expiration date of September 2027.
The recall record does not specify any remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Wellnov to request your refund or repair — edit it as you like.
Subject: Recall H-0797-2026 — Wellnov Wellnov Hello, I own a Wellnov that is covered by recall H-0797-2026 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.
