Medtronic Limited

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Description

5 devices in the database

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Medtronic Single Chamber Temporary External Pacemaker 53401
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Medtronic MiniMed Silhouette and MiniMed Sure-T infusion sets
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: [10 Oct 2013] Medtronic Model 8870 Software Application Card used in the 8840 N’Vision Clinician Programmer
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Medtronic SynchroMed Implantable Infusion Pump
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Medtronic Screw Module used with the ATLANTIS and Premier Anterior Cervical Plate System

2 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    HPRA
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Manufacturers representative
    Tamer frères S.A.L.
  • Source
    RLMPH