Progesterone 200 mg Capsules 90 capsules
Lack of Processing Control
Every FDA drug recall initiated in 2020, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
930 recalls, newest first.
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
Lack of Processing Control
CGMP Deviations: Impurity for N-nitroso-N-methyl-4-aminobutryric Acid (NBMA) detected in active ingredient (API) used to manufacture finished products.
Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.
Defective Delivery System: Out of specification for mechanical peel and shear.
Defective Delivery System: Out of specification for mechanical peel and shear.
Defective Delivery System: Out of specification for mechanical peel and shear.
Failed Impurities/Degradation Specification: Presence of unknown impurity observed.
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level