Cardiac Pacemakers Inc

17 dispositivos en la base de datos

  • Modelo / Serial
    Model: Models N107, P107, Affected: Devices manufactured prior to Dec-2009
  • Modelo / Serial
    Model: Models E102 & F102, Affected: Devices manfactured prior to Dec-2009
  • Modelo / Serial
    Model: Models N106, P106, Affected: Devices manufactured prior to Dec-2009
  • Modelo / Serial
    Model: Models E110 & F110, Affected: Devices manufactured prior to Dec-2009
  • Modelo / Serial
    Model: Models: E103 & F103, Affected: Manufactured prior to March 2010
12 más

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  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
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