Levocarnitine 100mg/Ml Mdv Soln
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
1,058 recalls, newest first
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Labeling: Not Elsewhere Classified; The packaging states these are ophthalmic drops. However, they are manufactured as nasal drops and sterility cannot be assured.
Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine
CGMP Deviations
Lack of Assurance of Sterility
Non-Sterility: firm's third party lab confirmed microbial contamination.
Failed Dissolution Specifications
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.
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.
Labeling: Not elsewhere classified: Mislabeling
Out of specification results for conductivity.
Failed Impurities/Degradation Specifications
Presence of foreign matter
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.
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NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
Lack of Assurance of Sterility: the manufacturing firm had microbial recoveries during environmental monitoring in aseptic areas of manufacturing.
Lack of sterility assurance
Failed Dissolution Specifications
Failed Viscosity Specifications: lot does not meet specification for Viscosity, which was determined through routine testing.
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.
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.
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.
Lack of Assurance of Sterility