Data / Product recalls / GnuPharma Corp.
GnuPharma Corp.: 1 recall in 2017 (FDA)
GnuPharma Corp., Owasso, OK, is named in 1 recall in 2017: all from the FDA. The latest, on July 26, 2017, covers GnuPharma Fit 100% Herbal Supplement 60 Capsules and 5 more products. Hazard: 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli). Source: FDA event 77506.
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- Country
- United States
- Location
- Owasso, OK
- Agencies
- U.S. Food and Drug Administration
- First recall
- July 26, 2017
- Latest recall
- July 26, 2017
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 |
|---|---|---|---|---|---|---|---|---|
| July 26, 2017 | FDA | GnuPharma Fit 100% Herbal Supplement 60 Capsules and 5 more products | 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) | 56 bottles (first of 6 products) | Voluntary recall, Class II, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 1 | July 26, 2017 |
Categories
| Category | Recalls |
|---|---|
| Beverages | 1 |
| Dietary supplements | 1 |
Where each agency publishes its recalls
Updated July 26, 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.