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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Loss of enzyme activity. these products maynot contain adequate enzyme activity for treatment of rec cells throughout the expiration dating of the product.
Model Catalog: (Lot serial: 212827 312878409928507979); Model Catalog: (Lot serial: LIC# 13482 CAT # 2310); Model Catalog: (Lot serial: SAME AS PREVIOUS); Model Catalog: (Lot serial: LOT EF50-1 LIC#13477CAT#7056); Model Catalog: (Lot serial: 122802205814219853); Model Catalog: (Lot serial: 305866319903402916); Model Catalog: (Lot serial: 416954430966); Model Catalog: (Lot serial: lic#13482); Model Catalog: (Lot serial: 514004)