The Recall Desk
SevereFDA (Food)·H-0796-2026·Announced 2026-05-27

FulviLife Complex Liquid Supplement Recalled for Bacterial Pathogen Risk

Wellnov Supplements LLC is recalling FulviLife Complex liquid supplement due to deviations from manufacturing standards that could allow bacterial pathogens and Clostridium botulinum to contaminate the product.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The FDA classified this as a Class II recall. The hazard involves high-risk pathogens (Clostridium botulinum) and bacterial contamination from cGMP deviations in a consumable product, which meets the threshold for Severe even without reported illnesses.

Plain-English summary

Wellnov Supplements LLC is recalling FulviLife Complex, a liquid supplement sold in 16 fl oz plastic bottles. The recall was initiated because the product was manufactured under conditions that deviated from current Good Manufacturing Practices (cGMP), creating potential for bacterial pathogen contamination and possible Clostridium botulinum concerns.

The affected product was distributed nationwide and in Puerto Rico with lot number FL1024, expiration date 10/2026, and distribution dates between 10/01/2024 and 04/08/2026. A total of 35 bottles were distributed.

Consumers who have purchased this product should stop using it immediately. Anyone who has consumed the product and experiences symptoms should contact a healthcare provider. Consumers may return the product to the place of purchase for a refund.

The recalled product

Product
FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Packaging: Plastic Bottle. Net Volume:16 fl oz (480 ml). Firm Address: VitaminAlly LLC Chandler, AZ 85225.
Manufacturer
Wellnov Supplements LLC
Hazard
  • bacterial-pathogen
  • clostridium-botulinum
  • manufacturing-deviation

Distribution

Distributed nationwide across the United States.