ARCHITECT "I" SYSTEM - ANTI-HBC II (DONOR SCREENING & CADAVERIC TESTING) REAGENT KIT

  • Model / Serial
    Model Catalog: 8L44-35 (Lot serial: 42256LI00 Exp Date 2015-06-30); Model Catalog: 8L44-25 (Lot serial: 42072LI00 Exp Date 2015-05-28); Model Catalog: 8L44-25 (Lot serial: 42256LI00 Exp Date 2015-06-30); Model Catalog: 8L44-35 (Lot serial: 42255LI01 Exp Date 2015-06-30); Model Catalog: 8L44-30 (Lot serial: 42255LI01 Exp Date 2015-06-30); Model Catalog: 8L44-25 (Lot serial: 42255LI01 Exp Date 2015-06-30); Model Catalog: 8L44-35 (Lot serial: 42255LI00 Exp Date 2015-06-30); Model Catalog: 8L44-30 (Lot serial: 42255LI00 Exp Date 2015-06-30); Model Catalog: 8L44-25 (Lot serial: 42255LI00 Exp Date 2015-06-30); Model Catalog: 8L44-35 (Lot serial: 42253LI01 Exp Date 2015-06-30); Model Catalog: 8L44-30 (Lot serial: 42253LI01 Exp Date 2015-06-30); Model Catalog: 8L44-25 (Lot serial: 42253LI01 Exp Date 2015-06-30); Model Catalog: 8L44-35 (Lot serial: 42253LI00 Exp Date 2015-06-30); Model Catalog: 8L44-30 (Lot serial: 42253LI00 Exp Date 2015-06-30); Model Catalog: 8L44-25 (Lot serial: 42253LI00 Exp Date 2015-06-30); Mod
  • Product Description
    ARCHITECT "I" SYSTEM - ANTI-HBC II (DONOR SCREENING & CADAVERIC TESTING) REAGENT KIT
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    MISSISSAUGA
  • 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
    HC