WARNING: Faulty Medication Recalled! 135 Batches of Potassium Capsules Pulled for Cardiac Arrest Risk!

Mumbai, India – A total of 135 batches of potassium chloride extended-release capsules are being recalled due to potential health risks that could result in cardiac arrest. The recall was initiated by Glenmark Pharmaceuticals, which pulled back 114 batches, and American Health Packaging, representing BluePoint Laboratories, recalled 21 batches of the same capsules, as reported by the US Food and Drug Administration. The capsules were recalled because of issues with capsule dissolution, which may lead …

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Blood Pressure Medication Recall: 135 Batches Removed for Dangerous Risk – FDA Urges Immediate Action

Miami, Florida – Over 130 batches of blood pressure medication have been recalled due to concerns that the pill capsules may not dissolve properly when taken by patients. Glenmark Pharmaceuticals recalls 114 batches of 750 mg Potassium Chloride contained in bottles with 100 and 500 pills, with the specific batch numbers and expiration dates detailed in a document circulated by the FDA. American Health Packaging also issued a voluntary recall of 21 batches of the …

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