The Recall Desk

Manufacturer

Darmerica, LLC

1 recall in our database name Darmerica, LLC as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
1
Severe
0
Most recent
2019-10-02

Of the 1 recalls from Darmerica, LLC 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-0125-2020·2019-10-02

    FDA Recalls Quinacrine Dihydrochloride Bulk API Due to Labeling Error

    Darmerica, LLC is recalling 1.8 kilograms of bulk Quinacrine Dihydrochloride API because testing revealed the product was actually Artemisinin.

    Product
    Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55, c) 25g NDC# 71052-530-25, Darmerica LLC 198 Wilshire Blvd Casselberry, FL 32707
    Category
    Drug
    Distribution
    Distributed nationwide