LIQUID BLENZ CORP Recalls Fibroid Bully 16 oz and 32 oz
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
LIQUID BLENZ CORP Recalls Fibroid Bully 16 oz and 32 oz
LIQUID BLENZ CORP · Class II — Moderate Risk

Product Description
Fibroid Bully 16 oz and 32 oz.
Reason for Recall
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
NY and online sales
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a food product from LIQUID BLENZ CORP, initiated on April 6, 2026. May be under-processed resulting in growth of Clostridium botulinum and lists health claims. This recall covers 18,190 bottles total, distributed in NY and online sales. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Food Contamination.