Wellnov recalls Liposomal D3+B12 Spray (30ml aluminum bottle) produced between Oct 2024 and Apr 2026 due to potential bacterial contamination. Consumers should check lot numbers and contact Wellnov for details.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Wellnov is recalling Liposomal D3+B12 Spray products made between October 2024 and April 2026 because of possible bacterial contamination risks. This recall is important because contaminated supplements could cause illness or serious health issues.
The products were made using Good Manufacturing Practices that deviated from standards, which could allow harmful bacteria to grow. This includes a potential risk of C. Botulinum, a serious bacterial infection that can cause food poisoning.
People who purchased the Liposomal D3+B12 Spray from Wellnov between October 2024 and April 2026. Those with compromised immune systems may be at higher risk from potential bacterial contamination.
Check for the aluminum bottle with 30ml capacity. Products were distributed from October 2024 to April 2026 with lot number DB1024 and expiry date October 2026.
Look for the aluminum bottle with 30ml capacity and lot number DB1024.
The recall states there is a potential risk of bacterial contamination, but the product is not confirmed unsafe. Consumers should check the lot number and contact Wellnov for details.
The recall record does not mention any remedy or replacement options. Consumers should contact Wellnov directly for assistance.
The product was distributed from October 1, 2024, to April 8, 2026.
We’ve drafted a message you can send Wellnov to request your refund or repair — edit it as you like.
Subject: Recall H-0806-2026 — Wellnov Wellnov Hello, I own a Wellnov that is covered by recall H-0806-2026 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.
