Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitamina
Summary
The FDA issued a Class II for Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Alumin by Wellnov Supplements LLC. Reason: Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns..
Details
Source
Food Recall
External ID
H-0798-2026
Action Date
2026-05-27
Status
Completed
Category
food
Product Description
Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
Lot/Code Info: Distribution dates: 10/01/2024-04/08/2026 Lot Number MM0925 Expiry Date 09/2027
Quantity Affected: 20 bottles
Reason for Recall
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Distribution
Products were distributed nationwide and the United States Territory of Puerto Rico.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-23
Company
Chandler, AZ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wellnov Supplements LLC has 14 FDA actions in our database, including 14 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wellnov Supplements LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wellnov Supplements LLC have FDA actions?
Wellnov Supplements LLC has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0798-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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