The HeartMate LVAS System Monitor allows clinicians to monitor performance of an implanted LVAD device. Screen issues may cause accidental pump stop.
Philips Respironics is updating the instructions for OmniLab Advanced+ (OLA+) Ventilator due to failure in the alarm, resulting in therapy interruption or loss.
Philips Respironics is updating the use instructions for V30, A30, and A40 ventilators due to failure in the alarm, resulting in therapy interruption or loss.
ZOLL Medical Corporation is updating instructions for 731 ventilators due to included MRI safety information, which may cause misuse and ventilator failure.
American Health Packaging on behalf of BluePoint Laboratories is voluntarily recalling 21 batches of Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, to the consumer level. The product is being recalled because of failed dissolution.Risk Statement: The failed dissolution of pot
Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ is voluntarily recalling 114 batches of Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, to the consumer level. The product is being recalled because of failed dissolution. Risk Statement: The failed dissolution of potassium chlor
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