FDA Drugs recall ·
Midodrine Hydrochloride Tablets, USP, 5 mg… recall
- Recall number
- D-0383-2026
- Date
- (initiated February 17, 2026)
- Company / brand
- The Harvard Drug Group LLC
7000 Cardinal Pl, Dublin, OH, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 8892 cartons
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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.
Why was it recalled?
Defective container; inadequately sealed blister packaging.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot # N02640, Exp Date: 08/2027
Distribution
Nationwide US.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0383-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.