Thallous Chloride TI 201 Injection
Chemical Contamination: Trace amounts of an impurity was detected in the reagent used to manufacture finished product.
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Chemical Contamination: Trace amounts of an impurity was detected in the reagent used to manufacture finished product.
Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.
Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.
Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.
Presence of Particulate Matter.
Presence of Particulate Matter.
Presence of Particulate Matter.
Failed pH Specification: product does not meet pH label claim.
Failed Impurities/Degradation Specifications: Out-of-specification results observed in related substance test (Any Other Individual Impurity and Total impurities) in Ethinyl Estradiol Tablets USP 0.01mg at 12 month long term stability study.
Labeling Not Elsewhere Classified; orange and cherry flavor packets incorrect list "natural lemon flavor" as an ingredient
Defective Container: firm discovered samples stored horizontally as well as product quality complaints from customers for bottles leaking.
Defective container: Ineffective seal between the cap and jar of the affected product.
Presence of Particulate Matter; glass particulates
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared ingredients: Sildenafil, Tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin, and daidzein.
CGMP Deviations; Detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) - N-Methylnitrosobutyric acid (NMBA).
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility