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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Teleflex is recalling these products as they may produce a straight stream instead of a fully atomized plume of medication. this may result in inadequate topical anesthesia which may lead to some discomfort further attempts to deliver topical anesthesia or the use of alternative methods of anesthesia.
Model Catalog: MAD510 (Lot serial: >10 lot # contact Mfg); Model Catalog: MAD500 (Lot serial: >10 lot # contact Mfg); Model Catalog: MAD600 (Lot serial: >10 lot # contact Mfg); Model Catalog: MAD700 (Lot serial: >10 lot # contact Mfg); Model Catalog: MAD720 (Lot serial: >10 lot # contact Mfg)