Deferoxamine 3300 mg/20 mL Sterile Water for Injection syringe
Lack of Sterility Assurance
Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.
14,543 recalls, newest first.
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance.
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance.
Lack of Sterility Assurance
Defective Container: Excess lidding material accumulation between the seal and the cup resulting in the lid not properly adhering and allowing leakage.
Discoloration: presence of atypical yellow discoloration of the solution .
Presence of Particulate Matter
Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain the correct statement of 0.9% benzyl alcohol added as a preservative.
Microbial Contamination of Non-Sterile Products: Failed S.aureus test.
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
Failed Impurities/Degradation Specifications; 12 month stability time point
Lack of Processing Controls
Lack of Processing Controls
Lack of Processing Controls
Lack of Processing Controls