Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
데이터 추가 비고
원인
Software malfunction causing liquid handling problems observed with magna pure lc 1.0 instrument (software version 3.0.11) and magna pure lc 2.0 instrument (software versions 1.1.23 and 1.1.24).
Model Catalog: 12236931001 (Lot serial: Software version 3.0.11); Model Catalog: 05197686001 (Lot serial: Software version v1.1.24); Model Catalog: 05197686001 (Lot serial: Software version v1.1.23)
제품 설명
MagNA Pure LC 1.0 Instrument - Software version 3.0.11