Liposomal Collagen Booster Recall Issued
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Wellnov Supplements LLC is recalling 49 bottles of Liposomal Collagen Booster due to cGMP deviations that could lead to bacterial pathogen and C. Botulinum concerns.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 10, 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
Liposomal Collagen Booster, 3mL liquid dosage in 90 ml aluminum bottle. 49 bottles affected. Lot Number CB0625, Expiry Date 06/2027. Distribution Dates: 06/01/2025-04/08/2026. Products distributed nationwide and to the United States Territory of Puerto Rico. Recall Number: H-0801-2026.
What You Should Do
Consumers should check product lot information and follow guidance from the recalling firm regarding the affected product.
Why This Matters
The recall involves potential bacterial contamination concerns in a dietary supplement distributed across the United States and Puerto Rico.
Source
FDA recall H-0801-2026 (Class II), initiated 2026-04-23.
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 (905 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.