Midodrine Hydrochloride 5 mg Recall
Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals
Updated February 17, 2026
Midodrine Hydrochloride Tablets 5 mg (50 tablets in blister packs) have been recalled due to inadequately sealed blister packaging. The defective container can compromise the integrity and safety of the medication.
Is the The Harvard Drug Group LLC recalled? Yes. This product was recalled by FDA on February 17, 2026. Details below.
What is recalled
Midodrine Hydrochloride Tablets, USP, 5 mg, 50 tablets (5 x 10 blister packs), NDC 0904-6818-06, packaged and distributed by Major Pharmaceuticals, Indianapolis, IN 46268.
Am I affected
You're affected if you have a prescription bottle or blister pack of Midodrine Hydrochloride Tablets 5 mg with NDC 0904-6818-06 packaged by Major Pharmaceuticals.
What to do right now
Stop taking this medication and contact your pharmacy or healthcare provider immediately. Do not use medication from a defective blister pack. Your doctor can provide a replacement or alternative medication.
The hazard
Defective container; inadequately sealed blister packaging.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0383-2026
- Classification
- Class II
- Recalled
- February 17, 2026
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