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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Due to a leak in the detector cooling system cooling liquid may leak outside the drip tray of the chiller. if this occurs the liquid may drip onto electrical components in the r-cabinet located in the technical room which could lead to damage to the system and potentially cause thermal events such as a burning odor smoke or fire.
Model Catalog: ALLURA XPER FD10/10 (Lot serial: ALL); Model Catalog: 722026 (Lot serial: ALL); Model Catalog: 001459 (Lot serial: ALL); Model Catalog: 722038 (Lot serial: ALL); Model Catalog: ALLURA XPER FD20 (Lot serial: ALL); Model Catalog: ALLURA XPER FD10 (Lot serial: ALL); Model Catalog: ALLURA XPER FD20/10 (Lot serial: ALL)