29 FDA recalls mention Aripiprazole. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Aripiprazole.
Reason Superpotent Drug: Product may not meet specifications throughout shelf life.
Reason Labeling:Label Mixup; ARIPiprazole, Tablet, 15 mg may be potentially mislabeled as ATOMOXETINE HCL, Capsule, 40 mg, NDC 00002322930, Pedigree…
Reason Labeling:Label Mixup; ARIPiprazole Tablet, 2 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree…
Reason CGMP Deviations: A drum of Abilify 30 mg Tablets rejected during the compression stage was not segregated from the other portion of the lot and was…
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