Class I · High risk
Vigabatrin for Oral Solution
Defective Container: powder may leak out of the pouch
Most common reason: cGMP deviation (1 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Vigabatrin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Defective Container: powder may leak out of the pouch
Cross contamination with other products
CGMP Deviations: recalling drug products following an FDA inspection.
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