Minoxidil 0.75%
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
14,450 recalls · Class II, newest first
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Reason Failed impurities/degradation specifications: Out of specification for unknown impurities.
Reason Failed Impurities/Degradations Specifications
Reason Failed Impurities/Degradation specifications
Reason Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Reason Failed Impurities/Degradation Specifications
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason Failed Impurities/Degradation Specifications: Failure observed in related substance testing during long term stability study.
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason cGMP Deviations
Reason CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
Reason Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.