Major Pharma Midodrine Tablets Recalled: Defective Packaging

This alert was compiled from official government recall data published by the FDA using automated analysis. All facts are sourced directly from official records. Last verified April 6, 2026.

So here's something you need to know about if you take Midodrine Hydrochloride tablets. The Harvard Drug Group LLC, doing business as Major Pharmaceuticals, is recalling a specific lot of its Midodrine Hydrochloride Tablets, USP, 5 mg. If you, or someone you know, uses this medication, sold across the U.S., pay close attention. This is a nationwide product recall in the United States, and it affects thousands of people.

Background: Midodrine Hydrochloride Tablets Recall

Midodrine Hydrochloride tablets are typically prescribed to treat low blood pressure. This particular product is packaged and distributed by Major Pharmaceuticals, located in Indianapolis, IN. As American shoppers know, medication safety is a serious matter, and recalls like this are put in place to protect you.

The Hazard: Defective Packaging

The reason for this product recall in the United States involves defective packaging. Specifically, the blister packaging, which is meant to keep the tablets sealed and protected, is not adequately sealed. Based on the official recall notice, this could compromise the integrity of the medication, potentially exposing it to moisture or other contaminants. Nobody wants to find out their medication is potentially compromised.

The agency confirmed that this issue affects 8892 cartons of the medication. This issue falls under a Class II recall, meaning that exposure to the affected product might cause a temporary or medically reversible adverse health consequence or where the probability of serious adverse health consequences is remote. This isn't The Harvard Drug Group's first recall, but this one involves a different product and a different problem.

Affected Product Details

Here's the specific information you need to check your medication:

• 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
• Lot Number: N02640
• Expiration Date: 08/2027

If you flip the product over, you'll find the lot number and expiration date printed on the packaging. Double-check that against the information above to see if your medication is affected.

Distribution Area

These Midodrine Hydrochloride tablets were distributed nationwide across the U.S. That means this recall affects people in every state, from California to New York, and everywhere in between. While specific retailers like Walmart, Target, Amazon, or Costco aren't mentioned in the recall, it's likely these tablets were available at various pharmacies and drug stores across the country.

What You Should Do Right Now

1. Stop using the Midodrine Hydrochloride Tablets with the affected lot number (N02640) immediately.
2. Contact your healthcare provider or pharmacist to discuss alternative medication options or address any concerns you may have. You can tell your doctor about the packaging issue and confirm it's safe to switch to a different lot or medication.
3. Return the affected medication to the pharmacy where you purchased it for proper disposal; do not flush the medication down the toilet or throw it in the trash.
4. Report any adverse reactions or quality problems experienced with the use of this product to the FDA's MedWatch Adverse Event Reporting program.

Frequently Asked Questions

Q: What does it mean that this is a Class II recall?

A Class II recall means that there is a reasonable probability that use of, or exposure to, a violative product will cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Q: How do I report an adverse reaction to the FDA?

You can report adverse reactions to the FDA's MedWatch program online, by phone, or by mail. Visit the FDA website for detailed instructions.

Q: What if I can't remember where I purchased the medication?

Even if you don't remember the exact pharmacy, contact any local pharmacy for guidance on proper disposal of the recalled medication. They can help you dispose of it safely.

Q: I have already taken some of the tablets from the affected lot. What should I do?

Consult your healthcare provider as soon as possible; they can assess any potential risks and advise you on the best course of action.

Q: How many recalls has the FDA issued this year?

The FDA has issued many recalls so far in 2026 across various product categories. Recalls are a common way for companies to address safety issues and ensure U.S. consumers are protected. You can check the FDA website for more information on recent recalls.

This recall was announced by the U.S. Food and Drug Administration (FDA). For the official notice and complete details, visit www.fda.gov.