Dextroamphetamine Saccharate
Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
11,818 recalls · Class II, newest first
Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
cGMP Deviations: deviations leading to potential cross-contamination.
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
Lack of Assurance of Sterility: Complaints received of defective container closure.
CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine (MNP) impurity.
Lack of Assurance of Sterility
Failed dissolution specifications.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Failed Dissolution Specifications: below specification limits for dissolution.
Failed Dissolution Specifications: below specification limits for dissolution.
Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets