💊 Drugs • 3,200 recalls
Omega & Delta Co.
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
MEDLINE INDUSTRIES, LP - Northfield
CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low assay results on the active ingredient miconazole nitrate.
Biomic Sciences, LLC
Microbial contamination of Non-Sterile Products
Biomic Sciences, LLC
Microbial contamination of Non-Sterile Products
Biomic Sciences, LLC
Microbial contamination of Non-Sterile Products
Dr. Berne's Whole Health Products
CGMP Deviations
Dr. Berne's Whole Health Products
CGMP Deviations
Dr. Berne's Whole Health Products
CGMP Deviations
Dr. Berne's Whole Health Products
CGMP Deviations
Dr. Berne's Whole Health Products
Non-Sterility
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Subpotent Drug: Product does not contain SPF that is declared on the label.
Subpotent Drug: Product does not contain SPF that is declared on the label.
AMMAN PHARMACEUTICAL INDUSTRIES
Lack of Assurance of Sterility
Incorrect/Undeclared Excipients.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations
CGMP Deviations: Products not manufactured under current good manufacturing practices.