Wellnov recalls Liposomal D3-5000IU spray 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 Liposomal D3-5000IU spray products that may contain bacterial pathogens or C. Botulinum risks due to manufacturing issues. This recall affects consumers who bought these supplements between October 2024 and April 2026.
The products were made with deviations from current Good Manufacturing Practices (cGMP), which could allow bacterial pathogens to grow. There is a potential risk for C. Botulinum, a serious bacterial infection that can cause food poisoning.
People who purchased the Liposomal D3-5000IU spray from Wellnov between October 2024 and April 2026 are affected. Those with health conditions that increase sensitivity to bacterial infections may be at higher risk.
Check for the aluminum bottle with 30 ml capacity labeled 'Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid'. Products were distributed from October 2024 to April 2026 with lot number DS1024.
Look for the aluminum bottle with 30 ml capacity labeled 'Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid'.
The recall states there is a potential risk for bacterial pathogens and C. Botulinum due to manufacturing deviations, so it is not safe to use.
The product was distributed from October 2024 to April 2026.
The recall does not specify a remedy, so you should contact Wellnov directly for guidance.
We’ve drafted a message you can send Wellnov to request your refund or repair — edit it as you like.
Subject: Recall H-0805-2026 — Wellnov Wellnov Hello, I own a Wellnov that is covered by recall H-0805-2026 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.
