Rasagiline Tablets 0.5mg
Failed dissolution specifications - results obtained were below spec average.
Most common reason: Dissolution failure (1 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Rasagiline. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Failed dissolution specifications - results obtained were below spec average.
Presence of Foreign Substance- A complaint was received of black spots/shiny metallic speck on the tablets.
Labeling:Label Mixup; RASAGILINE MESYLATE, Tablet, 0.5 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W002690, EXP: 6/5/2014.
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