Microplegia
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
775 recalls, newest first
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Product mixup: one foreign tablet found in product.
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Subpotent Drug: Out of specification results for low potency was obtained.
CGMP deviations.
CGMP deviations.
CGMP deviations.
CGMP deviations.
CGMP deviations.
Failed Impurities/Degradation Specifications: Above the specification limits yielded for related substance norepinephrine sulfonic acid impurity during routine product monitoring.
Sub-potent drug: assay test result below specifications at 9-month timepoint.
Chemical Contamination: FDA testing found Presence of methanol
Chemical Contamination: FDA testing found Presence of methanol
CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.
Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary packaging is incorrect.