Progressive Laboratories — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Progressive Laboratories has 4 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 23 Feb 2018. Progressive Laboratories is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Progressive Laboratories
How serious are Progressive Laboratories recalls?
FDA recall classifications by severity
Full FDA recall history for Progressive Laboratories
All 4 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 23 Feb 2018Official FDA Notice | Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap | Recalled dietary supplements may contain undeclared milk. | Class ITerminated |
| 23 Feb 2018Official FDA Notice | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap | Recalled dietary supplements may contain undeclared milk. | Class ITerminated |
| 23 Feb 2018Official FDA Notice | Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap | Recalled dietary supplements may contain undeclared milk. | Class ITerminated |
| 23 Feb 2018Official FDA Notice | Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap | Recalled dietary supplements may contain undeclared milk. | Class ITerminated |
Where have Progressive Laboratories recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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