Data / Product recalls / Basic Reset Inc.
Basic Reset Inc.: 1 recall in 2019 (FDA)
Basic Reset Inc., Hendersonville, TN, is named in 1 recall in 2019: all from the FDA. The latest, on November 27, 2019, covers BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F and 13 more products. Hazard: Products do not conform to Dietary Supplement CGMP regulations. Source: FDA event 83917.
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- Country
- United States
- Location
- Hendersonville, TN
- Agencies
- U.S. Food and Drug Administration
- First recall
- November 27, 2019
- Latest recall
- November 27, 2019
Recalls
Each recall is listed once, with the role this firm has in it. Roles: recalling firm (1).
| Date | Agency | Product | Hazard | Units | Remedy | Sold at | Role | Source |
|---|---|---|---|---|---|---|---|---|
| November 27, 2019 | FDA | BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F and 13 more products | Products do not conform to Dietary Supplement CGMP regulations. | 262 bottles (first of 14 products) | FDA Mandated recall, Class II, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 1 | November 27, 2019 |
Categories
| Category | Recalls |
|---|---|
| Beverages | 1 |
| Dietary supplements | 1 |
Where each agency publishes its recalls
Updated November 27, 2019. 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.