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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Defects may occur during the manufacturing of trima accel tubing sets. it was found during assembly of the ac/draw/return manifold the automated equipment may improperly insert the return line tubing into the manifold in such a way that the tubing maybe bent.
Model Catalog: 80700 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80450 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80500 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80490 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 777800-450 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80449 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80440 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80400 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 777800-550 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 777800-500 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 777800-400 (Lot serial: CONTACT MANUFACTURER FOR LOTS); Model Catalog: 80550 (Lot serial: CONTACT MANUFACTURER FOR LOTS)