Data / Product recalls / ProThera, Inc. dba SFI USA
ProThera, Inc. dba SFI USA: 2 recalls in 2019 (FDA)
ProThera, Inc. dba SFI USA, Reno, NV, is named in 2 recalls in 2019: all from the FDA. The latest, on April 3, 2019, covers Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7.... Hazard: Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate. Source: FDA F-1186-2019.
SpecStream is the live web data engine for teams and agents. It reads every recall from the CPSC, FDA and NHTSA each morning, and this page is that reading. Ask for the brands, categories or stores you follow and each new recall arrives in your sheet, CRM, Slack or agent as the agency publishes it.
- Country
- United States
- Location
- Reno, NV
- Agencies
- U.S. Food and Drug Administration
- First recall
- March 6, 2019
- Latest recall
- April 3, 2019
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 |
|---|---|---|---|---|---|---|---|---|
| April 3, 2019 | FDA | Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9 | Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate. | 139 bottles | Voluntary recall, Class II, terminated | Recalling firm | accessdata.fda.gov | |
| March 6, 2019 | FDA | Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE Bottle 60 Tablets UPC: 8 28054 17845 8; SKU: ML1 | Small quantity of product labeled as Melatonin Lozenge Formula were filled with L-Theanine. | 120 bottles | Voluntary recall, Class III, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 2 | April 3, 2019 |
Categories
| Category | Recalls |
|---|---|
| Dietary supplements | 2 |
Where each agency publishes its recalls
Updated April 3, 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.