10 FDA recalls mention Loxapine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Loxapine.
Reason GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross…
Reason GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross…
Reason CGMP Deviations
Reason CGMP Deviations
Reason Labeling: Label Mixup: LOXAPINE, Capsule, 5 mg may have potentially been mislabeled as the following drug: SERTRALINE HCL, Tablet, 50 mg, NDC…
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
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