Manufacturer
2 recalls in our database name Duy Drugs Inc. as the manufacturing or recalling firm.
Of the 2 recalls from Duy Drugs Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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.
Duy Drugs Inc. is recalling 411 bottles of Cardiovid Plus dietary supplements because they failed to meet FDA current good manufacturing practice requirements.
Duy Drugs Inc. is recalling 1,800 bottles of Viva ben Femenine Supplement because the product failed to meet current good manufacturing practices (CGMPs) for identity, purity, and composition.