Lorazepam Injection
Reason Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
14,450 recalls · Class II, newest first
Reason Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
Reason cGMP Deviations
Reason Failed Dissolution Specifications: potential for delayed dissolution of the dose after administration which may result in delayed release of the drug, delaying onset of sleep.
Reason Failed Dissolution Specifications: low dissolution results
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason Lack of Processing Controls.
Reason CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit
Reason CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations; particulates identified during visual inspection
Reason CGMP Deviations; particulates identified during visual inspection
Reason Subpotent Drug