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

VitaminAlly FulviLife Complex recalled over manufacturing practice deviations

VitaminAlly FulviLife Complex oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II recall where the manufacturing deviations are described as potentially leading to bacterial pathogen contamination, a named risk of harm with no illnesses reported.

Plain-English summary

FulviLife Complex, an oral liquid supplied in a 16 fl oz (480 ml) plastic bottle with a 2 tablespoon (30 ml) dose, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 35 bottles.

The stated reason is deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. botulinum concerns. The FDA classified the action as Class II.

The affected lot is FL1024, expiry 10/2026, distributed between 1 October 2024 and 8 April 2026. Distribution was nationwide and to Puerto Rico.

Consumers who have the affected lot should stop using it and dispose of it or return it to the place of purchase. Anyone who has used it and feels unwell should contact a healthcare provider.

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
Category
Food — Dietary supplement
Hazard
  • cgmp-deviation
  • bacterial-pathogen
  • clostridium-botulinum
  • class-ii

Distribution

Distributed nationwide across the United States.

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