GEM II DR

  • Model / Serial
    Model Catalog: 7273 (Lot serial: PJK200606H PJK200989H); Model Catalog: 7273 (Lot serial: PJK202209H PJK200857H); Model Catalog: 7273 (Lot serial: PJK200853H PJK201834H); Model Catalog: 7273 (Lot serial: PJK200322S PJK200611H); Model Catalog: 7273 (Lot serial: PJK200174H PJK200214H); Model Catalog: 7273 (Lot serial: PJK200743S PJK201835H); Model Catalog: 7273 (Lot serial: PJK200522S PJK200607H); Model Catalog: 7273 (Lot serial: PJK200346S PJK200521S); Model Catalog: 7273 (Lot serial: PJK200762S PJK200768S); Model Catalog: 7273 (Lot serial: PJK200415S PJK200305S); Model Catalog: 7273 (Lot serial: PJK201838H PJK201883H); Model Catalog: 7273 (Lot serial: PJK200424S PJK201837H); Model Catalog: 7273 (Lot serial: PJK200520S PJK201922H); Model Catalog: 7273 (Lot serial: PJK200310S PJK200524S); Model Catalog: 7273 (Lot serial: PJK200526S PJK200528S); Model Catalog: 7273 (Lot serial: PJK201815H PJK202178H); Model Catalog: 7273 (Lot serial: PJK200323S PJK200696S)
  • Product Description
    GEM DR II
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    BRAMPTON
  • 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
    HC