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
Potential contamination of a portion of tb antigen tubes from lot a111103n. tubes from this lot were subsequently included in the cellestis product t0590-0301 in the lots 59080161 and 59080171. it is suspected that the contamination may lead to higher rates of qft positive results.