Wellnov Supplements LLC Liposomal D3-5000IU Spray Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Wellnov Supplements LLC is recalling 88 bottles of Liposomal D3-5000IU Spray 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 initiated a voluntary recall due to 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 Liposomal D3-5000IU Spray (dosage: 3 sprays liquid in 30 ml aluminum bottle). 88 bottles are affected under lot number DS1024 (expiry 10/2026), distributed 10/01/2024-04/08/2026. Products were distributed nationwide and to Puerto Rico. Recall number: H-0805-2026. The recalling firm is Wellnov Supplements LLC, Chandler, AZ.
What You Should Do
Consumers should refer to FDA guidance for the ongoing recall (event ID 98832).
Why This Matters
This Class II recall addresses potential contamination risks in a dietary supplement distributed across the United States and Puerto Rico.
Source
FDA Recall H-0805-2026 - Wellnov Supplements LLC
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 (933 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.