Liquid Blenz Corp recalls 16oz and 32oz Immunity Enhancer Elderberry due to potential under-processing that could allow Clostridium botulinum growth. Consumers should check UPCs and contact the company for details.
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Liquid Blenz Corp is recalling their Immunity Enhancer Elderberry products (16 oz and 32 oz) because they may be under-processed, which could lead to harmful bacteria growth. This recall is important because under-processed elderberry products can pose a risk of serious illness if consumed.
Under-processed elderberry products can allow Clostridium botulinum bacteria to grow. This bacteria produces a toxin that can cause serious illness, including botulism, which is a rare but potentially life-threatening condition.
Anyone who purchased the 16 oz or 32 oz Immunity Enhancer Elderberry products with the listed UPCs. People who consume these products are at risk if the items were under-processed.
Check for the 16 oz product with UPC 860005735099 or the 32 oz product with UPC 195893965434. The recall does not specify the production lots.
Look for the 16 oz product with UPC 860005735099 or the 32 oz product with UPC 195893965434.
The recall states the products may be under-processed, which could lead to harmful bacteria growth. Consumers should not use these products until they are contacted by Liquid Blenz Corp.
The recall record does not specify any remedy for refunds or replacements.
The recall mentions a risk of Clostridium botulinum growth, which can cause serious illness including botulism.
We’ve drafted a message you can send Liquid Blenz Corp to request your refund or repair — edit it as you like.
Subject: Recall H-0787-2026 — Liquid Blenz Corp Liquid Blenz Corp Hello, I own a Liquid Blenz Corp that is covered by recall H-0787-2026 from Liquid Blenz Corp. 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.
