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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Hand controls manufactured before 06/2002 did not have vents. if the battery is damaged gases can build and split the case. some redesigned controls (assembled 06/2002-10/2003) had labels placed over the vents.
Model Catalog: AA1353 (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1353T (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1231U (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1336 (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1336L (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1320 (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1390U (Lot serial: ALL MANUFACTURED PRE-2003/10); Model Catalog: AA1380 (Lot serial: ALL MANUFACTURED PRE-2003/10)