4 FDA recalls mention Anagrelide. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Anagrelide.
Reason Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
Reason Failed Dissolution Specifications
Reason Failed Impurities/Degradation Specifications: High Out Of Specification results for impurities detected during routine stability testing.
Reason Labeling: Label Mixup: ANAGRELIDE HCL, Capsule, 0.5 mg may have potentially been mislabeled as the following drug: ARIPiprazole, Tablet, 2 mg, NDC…
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