Class III · Low risk
Nymalize (nimodipine)
Subpotent Drug
Most common reason: Failed specification (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Nimodipine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Subpotent Drug
Crystallization; crystallized nimodipine
Crystallization: Presence of crystals of Nimodipine within the capsule solution.
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