Boston Scientific

39 devices in the database

  • Model / Serial
  • Product Description
    Boston Scientific: Extractor Pro RX-S Retrieval Balloon Catheter
  • Model / Serial
  • Product Description
    Product name Models VALITUDE™ CRT-P U125, U128 ACCOLADE™ Pacemakers L300, L301, L310, L311, L321, L331 ESSENTIO™ Pacemakers L100, L101, L110, L111, L121, L131 VISIONIST™ CRT-P U225, U226, U228 PROPONENT™ Pacemakers L200, L201, L209, L210, L211, L221, L231 ALTRUA™ 2 Pacemakers S701, S702, S722In addition to the FSN which details affected product, please refer to the Excel spreadsheet below which accompanies this MDA for additional unique device identification information.
  • Model / Serial
  • Product Description
    Boston Scientific: ACCOLADE, ALTRUA 2, ESSENTIO, PROPONENT, VALITUDE, VISIONIST
  • Model / Serial
  • Product Description
    Boston Scientific: Advantage™ and Advantage Fit™ System, Transvaginal Sling, Lynx™ System, Suprapubic Sling Obtryx™ System, (Curved or Halo), Transobturator Sling, Obtryx™ II System with PrecisionBlue™ Design, (Curved or Halo), Transobturator Sling, Solyx™ SIS System, Single Incision Sling
  • Model / Serial
  • Product Description
    Boston Scientific: Capio™ SLIM Suture Capturing Device,
34 more

189 manufacturers with a similar name

Learn more about the data here

  • 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
    TDMDAT
  • 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
    TDMDAT
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
184 more