Manufacturer
45 recalls in our database name The Harvard Drug Group as the manufacturing or recalling firm.
Of the 45 recalls from The Harvard Drug Group we have scored against our rubric, 1 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 24 (53%) are Severe.
Which agencies issued them
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.
The Harvard Drug Group is voluntarily recalling Rugby Ferrous Sulfate Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby Liquid Vitamin C Supplement due to possible contamination with B. cepacia, which may cause serious infections.
The Harvard Drug Group is voluntarily recalling Major Tri-Vita Drops due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Major Poly-Vita Drops with Iron due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby Fer-iron Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Leader Liquid Multivitamin Supplement for Infants and Toddlers is being voluntarily recalled due to possible contamination with B. cepacia, which can cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby Calcionate Syrup due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Leader Liquid Vitamin D Supplement for Breastfed Infants is being voluntarily recalled due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby D 3 Vitamin Liquid due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
The Harvard Drug Group is voluntarily recalling Major D-Vita Drops due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling 914 cartons of Fluconazole 200 mg tablets because they failed to meet required dissolution specifications.
The Harvard Drug Group is recalling 2,341 cartons of Fluconazole 100 mg tablets because they failed to meet dissolution specifications.
The Harvard Drug Group is recalling Aripiprazole Tablets, 2 mg, due to out-of-specification assay results. The recall covers 36,990 tablets distributed nationwide and in Puerto Rico.
The Harvard Drug Group is recalling Diocto Liquid stool softener bottles due to positive findings of Burkholderia cepacia contamination.