Blood Pressure Medication Recalled Nationwide: See the Affected Drug
A commonly prescribed blood pressure medication has been recalled nationwide in the United States after the product failed a quality-control test that could affect how well the medicine works.
The medication involved is chlorthalidone 25 mg tablets, a prescription diuretic commonly used to help lower high blood pressure. According to reports citing the U.S. Food and Drug Administration (FDA), the latest recall involves 13,567 bottles distributed across the country.
Which Blood Pressure Medication Was Recalled?
The recalled medication is:
- Drug: Chlorthalidone Tablets, USP, 25 mg
- Manufacturer: Inventia Healthcare Limited
- Bottle size: 100 tablets
- NDC: 64980-599-01
- Lot/Batch: RISA24002
- Expiration date: April 2027
- Affected quantity: Approximately 13,567 bottles
The recall was initiated on September 3, 2026, after the tablets failed dissolution specifications. The FDA later classified the recall as Class II on September 17.
Why Was Chlorthalidone Recalled?
The issue involves dissolution testing.
Dissolution testing helps determine whether a tablet breaks down and releases its active ingredient at the expected rate. If a medication does not dissolve properly, the amount of medicine absorbed by the body may be affected.
For a blood pressure medication such as chlorthalidone, reduced or inconsistent absorption could potentially affect its intended effectiveness.
What Is Chlorthalidone Used For?
Chlorthalidone is a diuretic, sometimes called a water pill. It helps the body remove excess salt and water through urine and is used to help manage high blood pressure.
Because blood pressure treatment is often taken regularly, patients should not make sudden changes to their medication without speaking with a healthcare professional.
What Should Patients Do?
If you take chlorthalidone, check the information on your prescription bottle against the recalled product details above.
If your medication matches the recalled NDC, batch number, strength, and expiration date, contact your pharmacist or healthcare provider for guidance about a replacement or other appropriate action. EatingWell reports that consumers with an affected product can contact their pharmacy regarding replacement or refund options.
Do not stop taking prescribed blood pressure medication on your own. Contact your doctor or pharmacist before making changes to your treatment.
Is the Recall Dangerous?
The FDA's Class II designation means the recalled product may cause temporary or medically reversible health consequences, or that serious adverse effects are considered unlikely.
The recall does not mean that every bottle of chlorthalidone is affected. The recall applies to specific product information, including the identified batch and NDC number.
Patients who believe they have experienced a problem related to the medication should contact a healthcare professional.
Previous Chlorthalidone Recall
This is not the first recent chlorthalidone recall involving Inventia Healthcare.
In June 2026, another recall involving approximately 11,460 bottles of chlorthalidone 25 mg was announced after products also failed dissolution specifications. That recall involved different lots and product details.
Together, the two recalls involve more than 25,000 bottles of chlorthalidone.
How to Check Your Medicine
To determine whether your prescription is affected, look at the label on your bottle and compare:
Medication: Chlorthalidone Tablets, USP 25 mg
NDC: 64980-599-01
Batch: RISA24002
Expiration: 04/2027
Manufacturer: Inventia Healthcare Limited
If the information matches, speak with your pharmacist or healthcare provider for the next steps.
For the latest official information, consumers can also check the FDA's drug recall database and recall announcements.
Bottom Line
A nationwide recall affects 13,567 bottles of chlorthalidone 25 mg tablets manufactured by Inventia Healthcare Limited. The recall was initiated after the tablets failed dissolution specifications, which may affect how the medication is absorbed and potentially its effectiveness.
If you take chlorthalidone, check your bottle carefully. If it matches the recalled product information, contact your pharmacist or healthcare provider before making any changes to your medication.
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