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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An increase in ph may occur with some medications when instilled in the affected cassettes.This may lead to degradation of the drug which could result in diminished drug efficacy.
Model Catalog: 21-7100-24 (Lot serial: 081X16 TO 229X16); Model Catalog: 21-7002-24 (Lot serial: 081X16 TO 229X16); Model Catalog: 21-7001-24 (Lot serial: 081X16 TO 229X16)