Class IITerminatedVoluntary: Firm initiated
Armonia Natural Store LLC: food recall F-0221-2025
Armonia Natural Store LLC of Tamarac, FL recalled OneMultivitaminic GAF-PLUS Advance 300ml, plastic bottle, Room Temperature. Reason: Contains undeclared drugs Acetaminophen and Dexamethasone Phosphate, and the undeclared sweetener Aspartame. The FDA listed it as Class II in its Enforcement Report dated Dec 11, 2024; distribution: California, Florida, Georgia, Illinois, North Carolina, Nebraska, New Jersey, New York, Rhode Island, South Carolina, Virginia, Wisconsin.
Record status as published: Terminated (terminated Feb 19, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- OneMultivitaminic GAF-PLUS Advance 300ml, plastic bottle, Room Temperature
- Product quantity
- 64 Bottles
- Reason for recall
- Contains undeclared drugs Acetaminophen and Dexamethasone Phosphate, and the undeclared sweetener Aspartame
- Codes, lots and dates on the package
- Lot# 000297-0060724 Expiration Date:07/2026
- Distribution pattern
- Domestic distribution: FL, GA, NC, SC, RI, NY, NJ, VA, NE, IL, CA, WI
- Recalling firm
- Armonia Natural Store LLC, Tamarac, FL
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 6, 2024 |
| Classified by the FDA | Dec 2, 2024 |
| Published in the Enforcement Report | Dec 11, 2024 |
| Terminated | Feb 19, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0221-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.