Manufacturer
4 recalls in our database name Beta Labs as the manufacturing or recalling firm.
Of the 4 recalls from Beta Labs we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (75%) 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.
Beta Labs is recalling Phentylene capsules because they contain DMAA, a substance not permitted in dietary supplements.
Beta Labs is recalling 743 units of PHEnFX dietary supplements because they contain DMAA, a substance not permitted in dietary supplements.
Beta Labs is recalling Red Vipers dietary supplements because they contain DMAA, an ingredient not permitted in dietary supplements.
Beta Labs is recalling Oxyphen XR fat burner capsules because they contain DMAA, a substance not permitted in dietary supplements.