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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Braze joint within the shaft of the device may fail. tip may fall off or project from the delivery tube.
Model Catalog: 88372 (Lot serial: S/N 010201 TO 050215); Model Catalog: LM-900 (Lot serial: S/N 010201 TO 050215); Model Catalog: 50501 (Lot serial: S/N 010201 TO 050215); Model Catalog: 50502 (Lot serial: S/N 010201 TO 050215); Model Catalog: 88372 (Lot serial: S/N 110101 TO 110103); Model Catalog: 88372 (Lot serial: S/N 12744 TO 13500); Model Catalog: 50501 (Lot serial: S/N 110101 TO 110103); Model Catalog: 50502 (Lot serial: S/N 110101 TO 110103); Model Catalog: 50502 (Lot serial: S/N 12744 TO 13500); Model Catalog: 50501 (Lot serial: S/N 12744 TO 13500); Model Catalog: LM-900 (Lot serial: S/N 12744 TO 13500); Model Catalog: LM-900 (Lot serial: S/N 110101 TO 110103)