Manufacturer
4 recalls in our database name Progressive Laboratories, Inc as the manufacturing or recalling firm.
Of the 4 recalls from Progressive Laboratories, Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (50%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Progressive Laboratories is recalling Testosterzone dietary supplements because they may contain undeclared milk, a major food allergen.
Progressive Laboratories is recalling Thyroid Resilience dietary supplements because they may contain undeclared milk. Consumers should stop using the product and return it to the place of purchase.
Progressive Laboratories is recalling Xenesta Nuvive Men dietary supplements because they may contain undeclared milk.
Progressive Laboratories is recalling Xenesta Nuvive Women's 90-count bottles due to potential undeclared milk content.