Product: MIDODRINE HYDROCHLORIDE Classification: Class II Reason for recall: Defective container; inadequately sealed blister packaging. Product description: Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6818-06. Recalling firm: The Harvard Drug Group LLC Product type: Drugs
FDA MedWatch published a clinical safety alert in Pharmacology on 11 Mar 2026.
The item focuses on MIDODRINE HYDROCHLORIDE: Class II recall update.
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