The Recall Desk

Manufacturer

Blue Fusion Natural

1 recall in our database name Blue Fusion Natural as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
1
Severe
0
Most recent
2018-02-07

Of the 1 recalls from Blue Fusion Natural 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-0247-2018·2018-02-07

    Blue Pearl Capsules Recalled for Undeclared Sildenafil

    Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    BLUE PEARL capsules, 500mg, 1-count packets, Distributed by Blue Pearl Long Beach, CA UPC 8 4704600978 5
    Category
    Drug
    Distribution
    Distributed nationwide