FDA issues major recall of blood pressure medication due to cross

Check your medicine cabinets.

More than 11,100 bottles of a type of blood pressure medication sold under the brand name Ziac are being recalled due to cross-contamination with other medications, according to the U.S. Food and Drug Administration .

According to the FDA , the New Jersey-based Glenmark Pharmaceuticals recalled 11,136 bottles of bisoprolol fumarate and hydrochlorothiazide tablets because they had “traces of ezetimibe (a drug used to treat high cholesterol).”

No adverse effects have been reported to date.

READ MORE : FDA recalls 580K bottles of this blood pressure medication: Is your medicine on the list?

Here’s what you need to know about the recalled tablets — and what you should do if you have the recalled medication.

What Ziac tablets were subject to the recall?