The Recall Desk

Manufacturer

MS Bionic

1 recall in our database name MS Bionic as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
1
Severe
0
Most recent
2017-02-22

Of the 1 recalls from MS Bionic 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-0472-2017·2017-02-22

    MS Bionic Recalls MegaJex Herbal Supplement Containing Unapproved ED Drugs

    MS Bionic is recalling MegaJex Herbal Supplement because it contains sildenafil and tadalafil, active ingredients in approved erectile dysfunction drugs, without FDA approval.

    Product
    MegaJex Herbal Supplement, Maximum Formula for Men, Fast acting, Increase Stamina, 20 capsules, MS Bionics, Gardena, CA
    Category
    Drug
    Distribution
    1 state