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
Immucor is issuing this product notification regarding the v antigen typing for donor d1741 cell #4 on capture-r ready-id lot id324. further dna testing of donor d1741 has confirmed the donor as v- instead of v+ as indicated on the master list packaged with the product.