Liposomal Mens 50+ Liquid Multivitamin Drops Recall
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Wellnov Supplements LLC recalls 129 bottles of Liposomal Mens 50+ Liquid Multivitamin Drops 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.
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What Happened Wellnov Supplements LLC is recalling Liposomal Mens 50+ Liquid Multivitamin Drops 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 Liposomal Mens 50+ Liquid Multivitamin Drops (3mL liquid dosage in 90 ml aluminum bottles) distributed nationwide and in Puerto Rico. 129 bottles are affected under lot number M+0625 (expiry 06/2027) with distribution dates 06/01/2025-04/08/2026. The recalling firm is Wellnov Supplements LLC, Chandler, AZ; firm address listed as Vitaminally LLC, Chandler, AZ 85225. Recall number H-0799-2026. Classification: Class II.
What You Should Do Consumers should check product lot numbers against the recalled lot M+0625.
Why This Matters The recall affects products distributed across the United States and Puerto Rico, addressing potential contamination risks from manufacturing deviations.
Source FDA recall H-0799-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
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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 (1,029 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.