Levocarnitine 100mg/Ml Mdv Soln
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
17,898 recalls, newest first
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Labeling: Not Elsewhere Classified; The packaging states these are ophthalmic drops. However, they are manufactured as nasal drops and sterility cannot be assured.
Reason Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine
Reason CGMP Deviations
Reason Lack of Assurance of Sterility
Reason Non-Sterility: firm's third party lab confirmed microbial contamination.
Reason Failed Dissolution Specifications
Reason Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.
Reason Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.
Reason Labeling: Not elsewhere classified: Mislabeling
Reason Out of specification results for conductivity.
Reason Superpotent Drug
Reason Failed Impurities/Degradation Specifications
Reason Presence of foreign matter
Reason Non-Sterility - OOS sterility testing observed during 12-month controlled room temperature stability testing. The microbiological investigation identified the organism as a member of the Bacillus cereus group.
Reason Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
Reason Lack of Assurance of Sterility: the manufacturing firm had microbial recoveries during environmental monitoring in aseptic areas of manufacturing.
Reason Failed Stability Specifications; out of specification for shear.
Reason Failed Stability Specifications; out of specification for shear.
Reason Lack of sterility assurance
Reason Failed Dissolution Specifications
Reason Failed Viscosity Specifications: lot does not meet specification for Viscosity, which was determined through routine testing.
Reason CGMP Deviations: Out of specification (OOS) test result for Total Aerobic Microbial Count (TAMC) and Total Yeast and Mold Count (TYMC) for an excipient batch of Dibasic Calcium Phosphate.