Ablation

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “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.”
  • Source
    LAANSM

206 devices with a similar name

Learn more about the data here

  • Model / Serial
    D134701, D134702, D134703
  • Product Description
    For cardiac electrophysiological mapping, when used as a radiofrequency generator or for cardiac ablation.
  • Manufacturer
  • Model / Serial
    Model: All devices, Affected: All lots
  • Manufacturer
201 more