The Recall Desk

Manufacturer

HUMAN SCIENCE FOUNDATION

1 recall in our database name HUMAN SCIENCE FOUNDATION as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
1
Severe
0
Most recent
2014-05-28

Of the 1 recalls from HUMAN SCIENCE FOUNDATION we have scored against our rubric, 1 (100%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

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.

1–1 of 1

  • CriticalFDA (Drugs)·D-1327-2014·2014-05-28

    PRO ArthMax Dietary Supplement Recalled for Unapproved Active Ingredients

    Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.

    Product
    PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
    Category
    Drug
    Distribution
    Distributed nationwide