US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Feb 17, 2026 (7 months ago)

Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective container; inadequately sealed blister packaging.

What was recalled

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
NDC code
0904-6818-06
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0383-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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