The Impella device's catheter could cut through the wall of the left ventricle.
Vyaire recalls AirLife manual resuscitators because a manufacturing defect could result in patients not receiving enough ventilation, leading to injury or death.
Pyramid Wholesale is issuing a recall of various brands of products sold as dietary supplements for sexual enhancement because they contain undeclared prescription drugs including Sildenafil (Viagra) and/or Tadalafil (Cialis).
InfuTronix, LLC has announced a voluntary recall of the Nimbus Ambulatory Infusion Pump System, including Nimbus II PainPro, Nimbus II Flex, Nimbus II Plus, Nimbus II EpiD and Nimbus II EMS from the US Market due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump sys
Dans le traitement de la drépanocytose chez les patients de 12 ans et plus connaissant des crises vasoocclusives récurrentes.
L’exagamglogène autotemcel est indiqué dans le traitement de la thalassémie β dépendante aux transfusions (TDT) chez le patient de 12 ans ou plus.
Acute attacks of Type III Hereditary Angioedema (HAE nC1-INH).
Hampton, NH – On March 1, 2024, Sleepnet Corporation initiated a worldwide recall for all CPAP and BIPAP masks with magnets due to potential interference with certain medical devices. When a magnet comes into close proximity to certain medical implants or metallic implants, it could interfere with t
UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication
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