A popular blood pressure and kidney medication has been urgently recalled over concerns that capsules may not properly dissolve when ingested and lead to cardiac arrest. Glenmark Pharmaceuticals and American Health Packaging (on behalf of BluePoint Laboratories) voluntarily recalled 135 batches of Potassium Chloride. According to the FDA, Glenmark is pulling 114 batches of 750 mg of Potassium Chloride Extended-Release Capsules bottled with 100 and 500 pills. Click here for the batch numbers and expiration dates on recalled bottles of Glenmark Pharmaceuticals Potassium Chloride. American Health Packaging recalled 21 batches of 750 mg of Potassium Chloride Extended-Release Capsules bottled with 100 and 500 pills. Click here for the batch numbers and expiration dates on recalled bottles of American Health Packaging Potassium Chloride. Both manufacturers’ recalled products were sold nationwide. Speak To A Healthcare Provider About The Recalled Blood Pressure Medication The FDA announcements explained that if the capsules do not dissolve correctly, they can cause hyperkalemia. Someone with hyperkalemia—or elevated blood potassium levels—may experience an “irregular heartbeat that can lead to cardiac arrest” as well as cardiac arrhythmias and severe muscle weakness. If you’re having any of the above symptoms, seek medical attention immediately. If you are taking the recalled medication, the FDA asks that you speak to your doctor if you’re experiencing early hyperkalemia symptoms. The administration also suggests speaking to your healthcare provider before abruptly stopping your medication. You can find the source of this story’s featured image here. The post Common Blood Pressure Medication Recalled Nationwide appeared first on InspireMore.