Blood Pressure Drug Recall: Glenmark’s Ziac Contamination Alert
Patients taking Ziac for blood pressure control should check their prescriptions immediately. Glenmark Pharmaceuticals has recalled several lots of the drug after testing revealed contamination with ezetimibe, a cholesterol-lowering medication. The FDA has listed it as a “Class III recall: a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.”
What Is Being Recalled
The recall covers bisoprolol fumarate and hydrochlorothiazide tablets sold under the brand name Ziac. The affected products being recalled include:
30-tablet bottles — NDC 68462-878-30, Lot 17232401, exp. 11/2025
100-tablet bottles — NDC 68462-878-01, Lot 17232401, exp. 11/2025
500-tablet bottles — NDC 68462-878-05, Lot 17232401, exp. 11/2025
500-tablet bottles — NDC 68462-878-05, Lot 17240974, exp. 05/2026
If your bottle matches any of these details, it is part of the recall. If you are unsure, contact your pharmacist.
Why It Is Being Recalled
FDA testing found traces of ezetimibe in Ziac tablets. While ezetimibe is safe when prescribed for cholesterol, it should never appear in blood pressure medication. Cross-contamination violates strict manufacturing standards, and Glenmark has acted to remove the affected lots from circulation.
Patients should begin by examining their prescription bottle carefully. The lot number is normally printed near the expiration date. Compare the number on your bottle against the recalled lots, which are listed above and linked here. If you are uncertain about where to find the lot number or whether your medication is affected, call your pharmacist. He or she can confirm the details for you. Taking just a minute to check now could prevent an unnecessary risk later.
Next Steps If You Are Affected
If your medication matches one of the recalled lots, do not stop taking your medication. Contact your doctor or pharmacist promptly. He or she will discuss with you safe alternatives and guide you to make sure your blood pressure treatment continues without interruption. Once you have secured a replacement medication, given to you by your doctor or pharmacist.
Next, you will need to dispose of the recalled medication. Do not flush pills down the toilet or throw them in household trash. In order to properly dispose of the medication, use the pharmacy take-back program or follow FDA-approved disposal guidelines. If you have any unusual symptoms, report them immediately to the FDA’s MedWatch program. This prompt action allows regulators to track patient safety and respond quickly to needs and concerns.
This recall is a reminder of how carefully medications are monitored. Even small irregularities are taken seriously, which is why Glenmark acted quickly to remove the affected lots. The FDA has classified it as a Class III recall. This means it is low risk, and patients should feel confident that this is a precautionary measure. Check your bottles and follow up with your healthcare provider.
Disclaimer: This article is intended for informational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any questions or concerns you may have about your health or a medical condition. Never disregard professional medical advice or delay seeking it because of something you’ve read here.
