12 FDA recalls mention Nicardipine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Nicardipine.
Reason Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
Reason Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
Reason Lack of Assurance of Sterility.
Reason Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Reason Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Reason Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Subpotent Drug and Failed Impurities/Degradation Specifications
Reason Failed Impurity/Degradation Specifications; out of specification value for impurity Nitrophenylpuridine Derivative (NPP-D)
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