FulviLife Complex Recall Issued for cGMP Deviations
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Wellnov Supplements LLC is recalling 35 bottles of FulviLife Complex due to deviations from cGMP that could lead to bacterial pathogen and possible C. Botulinum concerns.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 11, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, food.
What Happened
Wellnov Supplements LLC is recalling FulviLife Complex because of deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Which Products Are Affected
The recall involves FulviLife Complex liquid supplement in 16 fl oz (480 ml) plastic bottles. Affected product has Lot Number FL1024 and Expiry Date 10/2026. A total of 35 bottles were distributed nationwide and to the United States Territory of Puerto Rico with distribution dates from 10/01/2024 to 04/08/2026.
What You Should Do
Consumers should follow instructions provided by the recalling firm for returns or refunds.
Why This Matters
The recall addresses potential risks associated with manufacturing deviations in a food product distributed across the United States and Puerto Rico.
Source
FDA recall number H-0796-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (888 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 11, 2026.
Frequently Asked Questions
Common questions about this FDA recall.