Data / Product recalls / Progressive Laboratories, Inc
Progressive Laboratories, Inc: 1 recall in 2018 (FDA)
Progressive Laboratories, Inc, Irving, TX, is named in 1 recall in 2018: all from the FDA. The latest, on March 21, 2018, covers Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap and 3 more products. Hazard: Recalled dietary supplements may contain undeclared milk. Source: FDA event 79350.
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- Country
- United States
- Location
- Irving, TX
- Agencies
- U.S. Food and Drug Administration
- First recall
- March 21, 2018
- Latest recall
- March 21, 2018
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 |
|---|---|---|---|---|---|---|---|---|
| March 21, 2018 | FDA | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap and 3 more products | Recalled dietary supplements may contain undeclared milk. | 669 bottles (first of 4 products) | Voluntary recall, Class I, terminated | Recalling firm | accessdata.fda.gov |
By agency
| Agency | Recalls | Latest |
|---|---|---|
| U.S. Food and Drug Administration | 1 | March 21, 2018 |
Where each agency publishes its recalls
Updated March 21, 2018. 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.