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.
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There have been recent complaints that the vitek 2 meropenem (mem mem02n) is overcalling resistance for isolates of aeromonas hydrophila. false resistance was confirmed when isolates from customer sites were tested internally by broth microdilution (bdm) the reference method used for development of mem02n.
Model Catalog: 413085 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413082 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413066 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413063 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413062 (Lot serial: ALL LOT NUMBERS); Model Catalog: 411021 (Lot serial: ALL LOT NUMBERS); Model Catalog: 410102 (Lot serial: ALL LOT NUMBERS); Model Catalog: 416710 (Lot serial: ALL LOT NUMBERS); Model Catalog: 414125 (Lot serial: ALL LOT NUMBERS); Model Catalog: 410101 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413710 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413143 (Lot serial: ALL LOT NUMBERS); Model Catalog: 413083 (Lot serial: ALL LOT NUMBERS)