Harvard Drug Group recalls Midodrine Hydrochloride 5 mg tablets over poorly sealed blister packs
The blister packs of these prescription tablets were not sealed properly, so the container is defective.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- 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.
- Company
- The Harvard Drug Group LLC
- Hazard
- Defective container; inadequately sealed blister packaging.
- Units
- 8892 cartons
- Where sold
- Nationwide US.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- March 3, 2026
- Recall started
- February 17, 2026
- FDA enforcement report
- March 11, 2026
- Identifiers
- Codes: Lot # N02640, Exp Date: 08/2027
- FDA recall number: D-0383-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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.
- Reason for recall
- Defective container; inadequately sealed blister packaging.
- Classification
- Class II (Ongoing)
- Distribution
- Nationwide US.
- Quantity
- 8892 cartons
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