Liquid Blenz Corp recalls Fibroid Bully 16 oz and : under-processed may grow botulism-causing bacteria. Consumers should check UPCs 860010984406 and 860010984413.
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Liquid Blenz Corp is recalling Fibroid Bully 16 oz and 32 oz products because they may be under-processed, potentially growing botulism-causing bacteria. This poses a health risk as botulism can cause serious illness.
Under-processed products may allow Clostridium botulinum bacteria to grow, which can produce botulinum toxin. This toxin causes botulism, a serious illness that can lead to paralysis and respiratory failure if not treated promptly.
Anyone who purchased Fibroid Bully 16 oz or 32 oz products with UPCs 860010984406 or 860010984413. People with compromised immune systems are at higher risk.
Check for UPCs 860010984406 (16 oz) or 860010984413 (32 oz) on the product label. The product is sold as Fibroid Bully 16 oz and 32 oz.
Immediately stop using and discard any Fibroid Bully 16 oz or 32 oz products with UPCs 860010984406 or 860010984413.
Liquid Blenz Corp is recalling Fibroid Bully 16 oz and 32 oz products because they may be under-processed, potentially growing botulism-causing bacteria.
Check for UPCs 860010984406 (16 oz) or 860010984413 (32 oz) on the product label.
Immediately stop using and discard the product.
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-0789-2026 — Liquid Blenz Corp Liquid Blenz Corp Hello, I own a Liquid Blenz Corp that is covered by recall H-0789-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
