Class II

Drug Recall: 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.

The Harvard Drug Group LLC · February 17, 2026

Reason for Recall

Defective container; inadequately sealed blister packaging.

Distribution

Nationwide US.

States Affected

NATIONWIDE

Quantity Affected

8892 cartons

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0383-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.