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.
ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
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If the internal aa batteries used to power the device leak their contents will cause damage to the device's internal components which may result in the device shutting off without issuing a warning or an audible or visual alarm. if the device shuts off it will result in a delay/interruption in therapy.
Model Catalog: 13150 (Lot serial: All Serial Numbers); Model Catalog: 13087 (Lot serial: All Serial Numbers); Model Catalog: 13088 (Lot serial: All Serial Numbers); Model Catalog: 13000 (Lot serial: All Serial Numbers)