Data / Product recalls / Sunset Natural Products Inc.
Sunset Natural Products Inc.: 2 recalls from 2016 to 2017 (FDA)
Sunset Natural Products Inc., Miami, FL, is named in 2 recalls from 2016 to 2017: all from the FDA. The latest, on January 4, 2017, covers Bionix, 30 capsules per bottle and 162 more products. Hazard: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or. Source: FDA event 74054.
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- Country
- United States
- Location
- Miami, FL
- Agencies
- U.S. Food and Drug Administration
- First recall
- February 24, 2016
- Latest recall
- January 4, 2017
Recalls
Each recall is listed once, with the role this firm has in it. Roles: recalling firm (2).
| Date | Agency | Product | Hazard | Units | Remedy | Sold at | Role | Source |
|---|---|---|---|---|---|---|---|---|
| January 4, 2017 | FDA | Bionix, 30 capsules per bottle and 162 more products | Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2... | 6,500 Bottles (195,000 capsules) (first of 163 products) | FDA Mandated recall, Class II, terminated | Recalling firm | accessdata.fda.gov | |
| February 24, 2016 | FDA | Abee Med, 60 capsules per bottle. Manufactured by Sunset Natural Products and 9 more products | Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2... | 3,149 bottles (240,000 caps) (first of 10 products) | FDA Mandated recall, Class II, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 2 | January 4, 2017 |
Categories
| Category | Recalls |
|---|---|
| Dietary supplements | 2 |
Where each agency publishes its recalls
Updated January 4, 2017. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.