St Jude Medical CRMD

44 devices in the database

  • Model / Serial
    All lots with a manufacturing date of May 30, 2006 or earlier
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • Product Description
    CPS Aim, Models 410140, 410141, 410142, 410144, 410145, 410146, 410147, & 410148
  • Model / Serial
    All lots with a manufacturing date of May 30, 2006 or earlier
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • Product Description
    CPS Implant Kit, Model 410190
  • Model / Serial
    All lots with a manufacturing date of May 30, 2006 or earlier
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • Product Description
    CPS Valve Bypass Tool (VBT), Model 410192
  • Model / Serial
    All lots with a manufacturing date of May 30, 2006 or earlier
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • Product Description
    CPS Slitter, Model 410191
  • Model / Serial
    All lots with a manufacturing date of May 30, 2006 or earlier
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • Product Description
    CPS Direct SL, Models 410110, 410111, 410112, 410113, 410114, 410115, 410116, 410120, 410121, 410122, 410123, 410124, 410125, & 410126
39 more

2 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    SMPA