Liposomal Kids Liquid Multivitamin Drops Recall
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Wellnov Supplements LLC is recalling 127 bottles of Liposomal Kids Liquid Multivitamin Drops due to cGMP deviations that could lead to bacterial contamination.
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 has initiated a voluntary recall of Liposomal Kids Liquid Multivitamin Drops 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 Kids Liquid Multivitamin Drops (3mL liquid dosage in 90 ml aluminum bottles) distributed nationwide and in Puerto Rico. Affected products have lot number KM0625, expiry date 06/2027, and were distributed between 06/01/2025 and 04/08/2026. A total of 127 bottles are affected. The recalling firm is Wellnov Supplements LLC, Chandler, AZ.
What You Should Do
Consumers should not use the recalled product. Contact information for returns or refunds is not specified in the recall notice.
Why This Matters
This Class II recall addresses potential contamination risks from manufacturing deviations in a children's supplement distributed across the United States and Puerto Rico.
Source
FDA recall number H-0802-2026 (event ID 98832).
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 (1,061 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.