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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These conditions may occur when liquid is present on the male or female parts of the luer connector before connection (resulting for example from use of disinfectant or drops of priming or dialysate solution) and the wet connector is screwed by using the body of the luer connectors for tightening instead of screwing the coupling nut. under these circumstances the fluid on the cone can act as a lubricant and might lead to an over-tightening of the connection. the resulting luer connection may be difficult to disconnect and the male luer lock may break when applying a high mechanical force.
Model Catalog: 800475 (Lot serial: ALL LOTS); Model Catalog: 800474 (Lot serial: ALL LOTS); Model Catalog: 003-800402 (Lot serial: ALL LOTS); Model Catalog: 002-800471 (Lot serial: ALL LOTS); Model Catalog: 800473 (Lot serial: ALL LOTS); Model Catalog: 800540 (Lot serial: ALL LOTS)