Hydravax High Potency Diuretic Weight Loss Solution — Class I drug recall D-1050-2014
Terminated recall by IQ Formulations, LLC, reported 2014-02-05, distributed nationwide. Marketed Without an Approved NDA/ANDA; this product is being recalled for containing an undeclared diuretic ca
| Recall number | D-1050-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | IQ Formulations, LLC, Sunrise, FL, United States |
| Recall initiated | 2013-11-04 |
| Classified | 2014-01-30 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2020-10-05 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
Product
Hydravax High Potency Diuretic Weight Loss Solution, Pharmaceutical Grade, 45 capsules per bottle, Dietary Supplement, Manufactured and Distributed by Metabolic Nutrition, Sunrise, Florida, www.metabolicnutrition.com
Reason for recall
Marketed Without an Approved NDA/ANDA; this product is being recalled for containing an undeclared diuretic called Triamterene, an FDA approved prescription only medication used to treat edema, making it an unapproved new drug
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1050-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.