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Medium risk Drugs & MedicationsClass II

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

The Harvard Drug Group LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0383-2026
Classification
Class II
Recalled
February 17, 2026
Read the official notice

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